T H Huisman

Author PubWeight™ 300.63^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins.	J Chromatogr	1965	4.17
2	Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.	Proc Natl Acad Sci U S A	1968	3.05
3	DNA sequence variation associated with elevated fetal G gamma globin production.	Blood	1985	2.41
4	Absence of messenger RNA and gene DNA for beta-globin chains in hereditary persistence of fetal hemoglobin.	Cell	1976	2.10
5	Studies on the heterogeneity of hemoglobin. 13. Chromatography of various human and animal hemoglobin types on DEAE-Sephadex.	J Chromatogr	1968	2.07
6	Globin chain electrophoresis: a new approach to the determination of the G gamma/A gamma ratio in fetal haemoglobin and to studies of globin synthesis.	Br J Haematol	1980	1.99
7	The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions.	Ann N Y Acad Sci	1974	1.99
8	Microchromatography of hemoglobins. II. A simplified procedure for the determination of hemoglobin A2.	J Lab Clin Med	1975	1.91
9	A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.	Proc Natl Acad Sci U S A	1986	1.80
10	Multiple cistrons for fetal hemoglobin in man.	Ann N Y Acad Sci	1974	1.53
11	Determination of the glycosylated hemoglobins (HB AI) with a new microcolumn procedure. Suitability of the technique for assessing the clinical management of diabetes mellitus.	Diabetes	1978	1.51
12	Detection of common deletional alpha-thalassemia-2 determinants by PCR.	Am J Hematol	1994	1.44
13	Normal fetal hemoglobin levels in the sudden infant death syndrome.	N Engl J Med	1989	1.42
14	An improved method for quantitative determination of human fetal hemoglobin.	Anal Biochem	1970	1.41
15	Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities.	Hemoglobin	1990	1.39
16	The detection of hemoglobin variants by isoelectrofocusing using EDTA-collected and filter paper-dried cord blood specimens.	Am J Clin Pathol	1990	1.39
17	The levels of abnormal hemoglobin in persons with heterozygosities for an alpha chain variant and for beta-thalassemia.	Hemoglobin	1997	1.38
18	Separation of human hemoglobins by DEAE-cellulose chromatography using glycine-KCN-NaC1 developers.	Hemoglobin	1977	1.32
19	Hemoglobin Kenya, the product of fusion of amd polypeptide chains.	Arch Biochem Biophys	1972	1.30
20	Homology requirements for unequal crossing over in humans.	Genetics	1991	1.27
21	Fetal erythropoiesis following bone marrow transplantation.	Blood	1976	1.26
22	Evidence for four nonallelic structural genes for the chain of human fetal hemoglobin.	Biochem Genet	1972	1.23
23	Sickle cell anemia and trait in southern India: further studies.	Am J Hematol	1979	1.20
24	Hemoglobin Richmond, a human hemoglobin which forms asymmetric hybrids with other hemoglobins.	J Biol Chem	1969	1.20
25	Hemoglobin Kenya, the product of a gamma-beta fusion gene: studies of the family.	Am J Hum Genet	1973	1.19
26	A new high-performance liquid chromatographic procedure to quantitate hemoglobin A1c and other minor hemoglobins in blood of normal, diabetic, and alcoholic individuals.	J Lab Clin Med	1983	1.19
27	Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients.	Blood	1984	1.18
28	Gamma thalassemia resulting from the deletion of a gamma-globin gene.	Nucleic Acids Res	1983	1.18
29	Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia.	N Engl J Med	1987	1.17
30	Evidence for multiple structural genes for the gamma-chain of human fetal hemoglobin in hereditary persistence of fetal hemoglobin.	Ann N Y Acad Sci	1969	1.17
31	A new high-performance liquid chromatographic procedure for the separation and quantitation of various hemoglobin variants in adults and newborn babies.	J Lab Clin Med	1983	1.16
32	Beta-thalassemia in Turkey.	Hemoglobin	1990	1.14
33	Gene deletion as the molecular basis for the Kenya-G gamma-HPFH condition.	Hemoglobin	1983	1.13
34	Qualitative and quantitative studies of sickle cell hemoglobin in homozygotes and heterozygotes.	Clin Chim Acta	1968	1.12
35	The heterogeneity of goat hemoglobin: evidence for the existence of two nonallelic and one allelic alpha chain structural genes.	Arch Biochem Biophys	1967	1.11
36	Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese families.	Blood	1985	1.10
37	Access to a syllabus of human hemoglobin variants (1996) via the World Wide Web.	Hemoglobin	1998	1.10
38	Microchromatography of hemoglobins. II. A rapid method for the determination of hemoglobin A2.	J Lab Clin Med	1974	1.10
39	Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain.	Biochem Genet	1984	1.09
40	Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes.	Proc Natl Acad Sci U S A	1986	1.08
41	The production of hemoglobin C in sheep carrying the gene for hemoglobin A: hematologic aspects.	Blood	1966	1.08
42	Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.	Am J Hum Genet	1977	1.06
43	Minor hemoglobins in sickle cell anemia, beta-thalassemia, and related conditions: a study of red cell fractions isolated by density gradient centrifugation.	Biochem Med	1975	1.06
44	The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes.	Blood	1984	1.04
45	Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia.	N Engl J Med	1971	1.03
46	Hemoglobin C in newborn sheep and goats: a possible explanation for its function and biosynthesis.	Pediatr Res	1969	1.03
47	Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.	Am J Hematol	1993	1.02
48	The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.	Hemoglobin	1991	1.01
49	Two novel polyadenylation mutations leading to beta(+)-thalassemia.	Br J Haematol	1990	1.01
50	alpha-Thalassaemia in the population of Cyprus.	Br J Haematol	1995	1.01
51	Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemia.	J Clin Invest	1971	1.01
52	Quantitation of hemoglobin components by high-performance cation-exchange liquid chromatography: its use in diagnosis and in the assessment of cellular distribution of hemoglobin variants.	Am J Hematol	1984	1.00
53	Molecular packing and intermolecular contacts of sickling deer type III hemoglobin.	J Mol Biol	1979	1.00
54	Upstream promoter mutation associated with a modest elevation of fetal hemoglobin expression in human adults.	Blood	1988	0.99
55	Hemoglobin Grady: the first example of a variant with elongated chains due to an insertion of residues.	Proc Natl Acad Sci U S A	1974	0.99
56	Pseudoautosomal repeat displays higher variability in blacks than in Caucasians.	Hum Genet	1992	0.99
57	Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation.	Br J Haematol	1992	0.99
58	The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults.	Mol Cell Biochem	1977	0.99
59	A homozygote for the Hb G type of foetal haemoglobin in India: a study of two Indian and four Negro families.	Br J Haematol	1972	0.98
60	Normal and abnormal human hemoglobins.	Adv Clin Chem	1972	0.98
61	Hemoglobin-Bibba or alpha-2-136Pro-beta 2, an unstable alpha chain abnormal hemoglobin.	Biochim Biophys Acta	1968	0.98
62	-G gamma A gamma-Thalassemia and gamma-chain variants in Chinese newborn babies.	Am J Hematol	1985	0.98
63	Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant.	Blood	1990	0.98
64	Molecular characterization of Hb S(C) beta-thalassemia in American blacks.	Am J Hematol	1991	0.98
65	gamma-Globin gene triplication and quadruplication in Japanese newborns. Evidence for a decreased in vivo expression of the 3'-A gamma-globin gene.	FEBS Lett	1985	0.97
66	Heterogeneity of fetal hemoglobin in beta-thalassemia of the Negro.	Am J Hum Genet	1970	0.96
67	Detection of alpha-thalassemia-2 (-3.7 kb) and its corresponding triplication (alpha)(alpha)(alpha) (anti-3.7 kb) by PCR: an improved technical change.	Am J Hematol	1996	0.96
68	Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.	Hemoglobin	1991	0.96
69	An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.	Blood	1989	0.96
70	Hb Grady and alpha thalassemia: a contribution to the problem of the number of Hb alpha structural loci in man.	Am J Hum Genet	1976	0.95
71	The levels of zeta, gamma, and delta chains in patients with Hb H disease.	Hum Genet	1989	0.95
72	Studies on the heterogeneity of hemoglobin. XIV. Chromatography of normal and abnormal human hemoglobin types on CM-Sephadex.	J Chromatogr	1969	0.95
73	Analysis of hemoglobin F production in Saudi Arabian families with sickle cell anemia.	Blood	1987	0.95
74	An electronic database of human hemoglobin variants on the World Wide Web.	Blood	1998	0.95
75	An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.	J Clin Invest	1971	0.94
76	World-wide occurrence of nonallelic genes for the -chain of human foetal haemoglobin in newborns.	Nat New Biol	1972	0.94
77	Trimodality in the percentages of beta chain variants in heterozygotes: the effect of the number of active Hbalpha structural loci.	Hemoglobin	1977	0.94
78	Haplotypes of beta S chromosomes among patients with sickle cell anemia from Georgia.	Hemoglobin	1986	0.94
79	Hemoglobin alpha chain deficiency in black children with variable quantities of hemoglobin Bart's at birth.	Pediatr Res	1977	0.93
80	Changes in the haemoglobin types of sheep as a response to anaemia.	Biochem J	1964	0.93
81	Two novel arrangements of the human fetal globin genes: G gamma-G gamma and A gamma-A gamma.	Nucleic Acids Res	1984	0.93
82	Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.	Acta Haematol	1989	0.93
83	Hemoglobin F in beta thalassemia and related conditions.	Ann N Y Acad Sci	1980	0.93
84	Homozygous hemoglobin O Arab in a gypsy family in Yugoslavia.	Hemoglobin	1977	0.93
85	A second type of hereditary persistence of foetal haemoglobin in India.	Br J Haematol	1973	0.93
86	A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.	Am J Hum Genet	1975	0.92
87	The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.	Br J Haematol	1994	0.92
88	Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition.	Blood	1981	0.92
89	A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian family.	Am J Hematol	1993	0.92
90	Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.	Br J Haematol	1989	0.92
91	Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin.	Nucleic Acids Res	1988	0.92
92	Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.	Acta Haematol	1994	0.92
93	Quantitation of hemoglobin alpha chains in adult and fetal goats; gene duplication and the production of polypeptide chains.	Arch Biochem Biophys	1969	0.91
94	The detection of beta-globin gene mutations in beta-thalassemia using oligonucleotide probes and amplified DNA.	Biochim Biophys Acta	1988	0.91
95	Non-synchronized suppression of postnatal activity in non-allelic genes which synthesize the Ggamma chain in human foetal haemoglobin.	Nat New Biol	1973	0.91
96	Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia.	J Clin Invest	1970	0.91
97	Alpha and beta thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization.	Br J Haematol	1994	0.90
98	Anomaly in the gamma chain heterogeneity of the newborn.	Nature	1977	0.90
99	Types of alpha-globin gene deficiencies in Chinese newborn babies in the Guangxi region, P. R. China.	Hemoglobin	1992	0.90
100	Homozygous beta0- and beta+ - thalassemia in Kurdish Jews and Arabs.	Hemoglobin	1977	0.90
101	Dutch beta 0-thalassaemia: a 10 kilobase DNA deletion associated with significant gamma-chain production.	Br J Haematol	1984	0.90
102	The structure of goat hemoglobins. I. Structural studies of the beta chains of the hemoglobins of normal and anemic goats.	J Biol Chem	1967	0.90
103	Polymorphic pattern of the (AT)X(T)Y motif at -530 5' to the beta-globin gene in over 40 patients homozygous for various beta-thalassemia mutations.	Am J Hematol	1994	0.89
104	The ratio of the G gamma and A gamma chains: variations due to anomalies at the molecular level.	Ann N Y Acad Sci	1985	0.89
105	The T gamma chain of human fetal hemoglobin at birth and in several abnormal hematologic conditions.	Pediatr Res	1977	0.89
106	On the chromatographic heterogeneity of human fetal hemoglobin.	Biochim Biophys Acta	1979	0.89
107	Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family.	Hemoglobin	1988	0.89
108	One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.	Blood	1989	0.88
109	The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.	Biochim Biophys Acta	1996	0.88
110	Hemoglobin Freiburg: abnormal hemoglobin due to deletion of a single amino acid residue.	Science	1966	0.88
111	Nature of foetal haemoglobin in F-thalassaemia.	Br J Haematol	1971	0.88
112	Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.	Clin Chim Acta	1972	0.87
113	Hb E and Hb E-like variants in individuals from Turkey.	Hemoglobin	1981	0.87
114	A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central Portugal.	Br J Haematol	1992	0.87
115	Molecular characterization of beta-thalassemia in north Jordan.	Hemoglobin	1994	0.87
116	Hemoglobin Savannah (B6(24) beta-glycine is greater than valine): an unstable variant causing anemia with inclusion bodies.	J Clin Invest	1971	0.87
117	A fetal hemoglobin with abnormal gamma-polypeptide chains: hemoglobin Warren.	Blood	1965	0.87
118	The occurrence of different levels of G gamma chain and of the A gamma T variant of fetal hemoglobin in newborn babies from several countries.	Am J Hematol	1983	0.87
119	Microchromatography of hemoglobins. IV. An improved procedure for the detection of hemoglobins S and C at birth.	J Lab Clin Med	1975	0.87
120	The hemoglobin heterogeneity of the Virginia white-tailed deer: a possible genetic explanation.	Arch Biochem Biophys	1968	0.87
121	The in vivo production of hemoglobin C in ruminants.	Ann N Y Acad Sci	1974	0.87
122	Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography.	J Chromatogr	1986	0.87
123	Search for nonallelic structural genes for gamma-chains of fetal hemoglobin in some primates.	Biochem Genet	1973	0.86
124	A novel deletion of approximately 27 kb including the beta-globin gene and the locus control region 3'HS-1 regulatory sequence: beta zero-thalassemia or hereditary persistence of fetal hemoglobin?	Blood	1994	0.86
125	The Ggamma deltabeta-thalassemia and Ggamma-betaO-hpfh conditions in combination with beta-thalassemia and Hb S.	Am J Hematol	1977	0.86
126	Oxygen equilibria studies of the hemoglobins from normal and anemic sheep and goats.	Am J Physiol	1968	0.86
127	Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from Kenya.	Br J Haematol	1987	0.86
128	The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesis.	Am J Hematol	1979	0.85
129	Fetal hemoglobin in normal adults and beta-thalassemia heterozygotes.	Hum Genet	1990	0.85
130	Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.	Br J Haematol	1989	0.85
131	The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin.	Blood	1994	0.85
132	An adult homozygous for persistent fetal hemoglobin.	Ann Intern Med	1970	0.85
133	Quantitative microchromatographic determination of hemoglobin F in patients with hemoglobins S and/or C.	Am J Hematol	1976	0.85
134	Radioimmunoassay for abnormal hemoglobins.	Science	1977	0.85
135	A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----Tyr.	Hemoglobin	1992	0.84
136	Beta-thalassemia due to a T----A mutation within the ATA box.	Biochem Biophys Res Commun	1988	0.84
137	The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene.	Blood	1991	0.84
138	Structural characterization of two delta chain variants. Hemoglobin A'-2 (B2) and hemoglobin Flatbush.	J Biol Chem	1967	0.84
139	Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.	Biochem Genet	1982	0.84
140	Experiences with the quantitation of human hemoglobin types by high pressure liquid chromatography.	Prog Clin Biol Res	1981	0.84
141	Hb Vaasa or alpha2beta2 (39(C5)Gln replaced by Glu), a mildly unstable variant found in a Finnish family.	Hemoglobin	1977	0.84
142	Red cell 2,3-diphosphoglycerate and oxygen affinity in newborn goats and sheep.	Proc Soc Exp Biol Med	1971	0.84
143	Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114.	Blood	1988	0.84
144	Allele-specific amplification for the identification of several hemoglobin variants.	Hemoglobin	1993	0.84
145	Gene structure in hereditary persistence of fetal hemoglobin individuals.	Hemoglobin	1980	0.83
146	The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C----G substitution at nucleotide -195 of the A gamma-globin gene.	Blood	1990	0.83
147	(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA.	Br J Haematol	1985	0.83
148	alpha Chain and gamma chain abnormal hemoglobins in newborn babies: structural and genetic aspects.	Am J Hematol	1983	0.83
149	Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns.	Am J Hum Genet	1986	0.83
150	An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta-thalassemia.	Blood	1987	0.83
151	Hb Alesha or alpha 2 beta (2)67(E11)Val-->Met: a new unstable hemoglobin variant identified through sequencing of amplified DNA.	Hemoglobin	1993	0.83
152	Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure.	Blood	1988	0.83
153	Studies on the heterogeneity of hemoglobin. XI. Chromatographic studies of intermediate forms of oxy- and ferrihemoglobin.	Arch Biochem Biophys	1966	0.83
154	Characterization of the beta+-thalassemia mutation in a homozygous Yugoslavian patient.	Hemoglobin	1984	0.83
155	Separation of hemoglobins and hemoglobin chains by high-performance liquid chromatography.	J Chromatogr	1987	0.83
156	Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes.	Blood	1991	0.83
157	Five adults with mild sickle cell anemia share a beta S chromosome with the same haplotype.	Am J Hematol	1985	0.83
158	The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence.	Br J Haematol	1989	0.83
159	International Hemoglobin Information Center variant list.	Hemoglobin	1996	0.82
160	The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotes.	Am J Clin Pathol	1981	0.82
161	New aspects of the structure, function, and synthesis of hemoglobins.	CRC Crit Rev Clin Lab Sci	1970	0.82
162	The chemical heterogeneity of the fetal hemoglobin of black newborn babies and adults: a reevaluation.	Blood	1981	0.82
163	The beta-delta crossover leading to the beta delta hybrid gene of hemoglobin P-Nilotic is located within 54 base-pairs of the 5' end of exon 2 or between codons 31 and 50.	Biochim Biophys Acta	1987	0.82
164	The use of globin chain electrophoresis in polyacrylamide gels for the quantitation of the G gamma to A gamma ratio in fetal hemoglobin.	Hemoglobin	1981	0.82
165	Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.	Hemoglobin	1989	0.82
166	Studies of the proporation and synthesis of haemoblogin C Philadelphia in red cells of heterozygotes, a homozygote, and a heterozygote for both haemoglobin G and alpha thalassaemia.	Br J Haematol	1976	0.82
167	Homozygosity for a new type of G gamma (A gamma delta beta)zero-thalassemia in a Malaysian male.	Hemoglobin	1986	0.82
168	First observation of hemoglobin J Paris I [alpha-2-12(A10)alanine-aspartic acid beta-2] in the Indian subcontinent.	Acta Haematol	1988	0.82
169	Subunit dissociation of the abnormal hemoglobins G Georgia ( 2 95Leu (G2) 2 ) and Rampa ( 2 95Ser (G2) 2 ).	J Biol Chem	1972	0.82
170	Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes.	Blood	1992	0.82
171	Partial deletion of the 5' beta-globin gene region causes beta zero-thalassemia in members of an American black family.	Blood	1984	0.82
172	Hb Tigraye or alpha 2 beta (2)79(EF3)Asp-->His(GAC-->CAC): a hemoglobin variant with increased oxygen affinity observed in an Ethiopian male.	Hemoglobin	1993	0.82
173	Two different theta (theta) globin gene deletions observed among black newborn babies.	Br J Haematol	1988	0.82
174	Recent advances in the quantitation of human fetal hemoglobins with different gamma chains.	Am J Hematol	1980	0.82
175	Homozygotes for the hereditary persistence of fetal hemoglobin: the ratio of G gamma to A gamma chains and biosynthetic studies.	Biochem Genet	1977	0.82
176	Delta beta-thalassemia in a Mexican family: clinical differences among homozygotes.	Hemoglobin	1978	0.82
177	The influence of antiserum to human erythropoietin on the production of hemoglobin C in goats.	Proc Soc Exp Biol Med	1970	0.81
178	Molecular characterization of beta-thalassemia in Azerbaijan.	Hum Genet	1992	0.81
179	A large beta-thalassemia deletion in a family of Indonesian-Malay descent.	Hemoglobin	1996	0.81
180	On the quaternary structure of hemoglobin A-Ic.	Biochim Biophys Acta	1969	0.81
181	A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia.	Int J Hematol	1991	0.81
182	Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variants.	Hemoglobin	1997	0.81
183	Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.	Hemoglobin	1985	0.81
184	Further studies of the frequency and significance of the Tgamma-chain of human fetal hemoglobin.	J Clin Invest	1979	0.81
185	A possible subclass of the hereditary persistence of fetal hemoglobin.	Blood	1970	0.81
186	Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.	Am J Hematol	1992	0.81
187	Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu----Gln in a Czechoslovakian male.	Hemoglobin	1986	0.81
188	Low pulse oximeter-measured hemoglobin oxygen saturations with hemoglobin Cheverly.	Am J Hematol	1998	0.81
189	One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.	Hum Genet	1987	0.81
190	Mechanism of sickling in deer erythrocytes.	Ann N Y Acad Sci	1974	0.81
191	Different zeta globin gene deletions among black Americans.	Hum Genet	1986	0.81
192	Hemoglobin Hamadan or alpha 2 beta 256(D7)Gly----Arg in a Turkish family.	Hemoglobin	1984	0.81
193	Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family.	Hemoglobin	1989	0.81
194	Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya.	Hum Genet	1987	0.80
195	Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observations.	Br J Haematol	1986	0.80
196	Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations.	Hum Genet	1994	0.80
197	Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18).	Biochim Biophys Acta	1975	0.80
198	Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant.	Hemoglobin	1989	0.80
199	The V gamma chain of fetal hemoglobin of the orangutan.	Biochem Genet	1978	0.80
200	Chinese in west Malaysia: the geography of beta thalassaemia mutations.	Singapore Med J	1990	0.80
201	A de novo deletion causing epsilon gamma delta beta-thalassemia in a Dutch patient.	Acta Haematol	1996	0.80
202	Four categories of gamma-globin gene triplications: DNA sequence comparison of low G gamma and high G gamma triplications.	Blood	1988	0.80
203	Delta Beta-Thalassaemia in two yugoslavian families.	Scand J Haematol	1975	0.80
204	Two arrangements of the human fetal globin genes may be responsible for high G gamma values in Chinese newborns: -G gamma-G gamma-delta-beta and -G gamma-A gamma G gamma-A gamma-delta-beta.	Am J Hematol	1985	0.80
205	gamma-mRNA and Hb F levels in beta-thalassaemia.	Br J Haematol	1994	0.80
206	Another form of the hereditary persistence of fetal hemoglobin (the Atlanta type)?	Hemoglobin	1977	0.80
207	Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.	Biochim Biophys Acta	1992	0.80
208	Minor hemoglobins in sickle-cell heterozygotes and homozygotes with and without diabetes.	Biochim Biophys Acta	1980	0.80
209	Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation.	Genomics	1998	0.80
210	HB F-Yamaguchi (gamma 75Thr, gamma 80Asn, gamma 136Ala) is associated with G gamma-thalassemia.	Am J Hematol	1984	0.79
211	A G to A nucleotide substitution 161 base pairs 5' of the G gamma globin gene cap site (-161) in a high G gamma non-anemic person.	Prog Clin Biol Res	1987	0.79
212	Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.	Hemoglobin	1989	0.79
213	Amino acid sequences in the -chains of adult bovine hemoglobins C-Rhodesia and D-Zambia.	Arch Biochem Biophys	1972	0.79
214	Rapid cation-exchange high-performance liquid chromatographic procedure for the separation and quantitation of hemoglobins S, C, and O Arab in cord blood samples.	J Lab Clin Med	1986	0.79
215	The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography.	Hemoglobin	1984	0.79
216	The heterogeneity of the fetal hemoglobin of the goat.	Biochim Biophys Acta	1969	0.79
217	Molecular characterization of beta-thalassemia in Hungary.	Hum Genet	1993	0.79
218	Differences in affinity of variant beta chains for alpha chains: a possible explanation for the variation in the percentages of beta chain variants in heterozygotes.	Hemoglobin	1977	0.79
219	Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populations.	Hemoglobin	1993	0.79
220	IV. The chemical heterogeneity of the chain from human fetal hemoglobin.	CRC Crit Rev Clin Lab Sci	1970	0.79
221	Reverse dot-blot detection of the African-American beta-thalassemia mutations.	Blood	1995	0.79
222	Hb Icaria-Hb H disease: identification of the Hb Icaria mutation through analysis of amplified DNA.	Br J Haematol	1990	0.79
223	A novel alpha-thalassemia-2 (-2.7-kb) observed in a Chinese patient with Hb H disease.	Am J Hematol	1991	0.79
224	The amino acid sequence of the delta-beta chains of hemoglobin Lepore Augusta = Lepore Washington.	Biochim Biophys Acta	1966	0.79
225	Certain mutations observed in the 5' sequences of the G gamma- and A gamma-globin genes of beta S chromosomes are specific for chromosomes with major haplotypes.	Acta Haematol	1991	0.79
226	Hb-J-Georgia=Hb-J-Baltimore= 2 2 16 Gly leads to Asp.	Clin Chim Acta	1971	0.79
227	Five haplotypes in Black beta-thalassaemia heterozygotes: three are associated with high and two with low G gamma values in fetal haemoglobin.	Br J Haematol	1985	0.79
228	Hydroxyurea therapy in sickle cell anemia patients in Curaçao, The Netherlands Antilles.	Acta Haematol	1997	0.79
229	High frequencies of a rearrangement (+ATA; -T) at -530 to the beta-globin gene in different populations indicate the absence of a correlation with a silent beta-thalassemia determinant.	Hemoglobin	1989	0.79
230	First observation of haemoglobin Malay alpha 2B2 26 (B1) Asn----Ser--a case report.	Med J Malaysia	1989	0.79
231	Chromatographic separation of hemoglobins A 2 and C. The quantities of hemoglobin A 2 in patients with AC trait, CC disease, and C- -thalassemia.	Clin Chim Acta	1972	0.79
232	The heterogeneity of the gamma-chain of fetal hemoglobin in HbS heterozygotes.	Blood	1982	0.79
233	Hemoglobin Istanbul: substitution of glutamine for histidine in a proximal histidine (F8(92) ).	J Clin Invest	1972	0.78
234	A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian family.	Hemoglobin	1992	0.78
235	The structure of goat hemoglobins. IV. A third beta chain variant (betaE) with three apparent amino acid substitutions.	Arch Biochem Biophys	1970	0.78
236	Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults.	Biochem Genet	1977	0.78
237	Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31.	Hemoglobin	1985	0.78
238	Hb Costa Rica or alpha 2 beta 2 77(EF1)His --> Arg: the first example of a somatic cell mutation in a globin gene.	Hum Genet	1996	0.78
239	Hemoglobin St Luke's, or alpha 2 , 95 Arg (G2) beta 2 .	Eur J Biochem	1972	0.78
240	Hb F-La Grange or alpha 2 gamma 2 101(G3)Glu----Lys; 75Ile; 136Gly: a high oxygen affinity fetal hemoglobin variant observed in a Caucasian newborn.	Biochim Biophys Acta	1984	0.78
241	Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplication.	Am J Hum Genet	1986	0.78
242	The synthesis of the G gamma and A gamma chains of human fetal hemoglobin in erythroid colonies cultured from peripheral blood BFUe's of normal adults and newborn and of subjects with an A gamma or a G gamma chain abnormal fetal hemoglobin.	Am J Hematol	1980	0.78
243	Subunit dissociation of the unstable hemoglobin Bibba (alpha 2-136Pro(H19)beta 2).	J Biol Chem	1970	0.78
244	An initiation codon mutation as a cause of a beta-thalassemia.	Hemoglobin	1990	0.78
245	Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.	Acta Haematol	1992	0.78
246	Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.	Ann Hematol	1991	0.78
247	Radioimmunochemical characterization of hemoglobins Lepore and Kenya: unique antigenic determinants located on hybrid hemoglobins.	J Immunol	1978	0.78
248	Sickle cell anemia as a syndrome: a review of diagnostic features.	Am J Hematol	1979	0.78
249	Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene.	Br J Haematol	1991	0.78
250	Hemoglobin H disease in two Turkish females and one Iranian newborn.	Hemoglobin	1985	0.78
251	Hb Setif or alpha 2 94(G1)Asp----Tyr beta 2 observed in a Saudi Arabian family.	Hemoglobin	1985	0.78
252	Hb Wayne, the frameshift variant with extended alpha chains observed in a Caucasian family from Alabama.	Hemoglobin	1984	0.78
253	Hemoglobin A2-Indonesia or alpha 2 delta 2 69(E13) Gly--Arg.	Biochim Biophys Acta	1971	0.78
254	Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotes.	Hemoglobin	1981	0.78
255	Hb Graz or alpha 2 beta 2(2)(NA2)His-->Leu; a new beta chain variant observed in four families from southern Austria.	Hemoglobin	1992	0.78
256	Variability in the fetal hemoglobin level of the normal adult.	Am J Hematol	1996	0.78
257	Recombinant hemoglobin variants.	Hemoglobin	1998	0.78
258	Specific radioimmunochemical identification and quantitation of hemoglobins A2 and F.	Am J Hematol	1976	0.78
259	Hb F-Dammam or alpha 2A gamma 2(79) (EF3) Asp----Asn.	Hemoglobin	1985	0.78
260	Hemoglobin Russ or alpha-2-51-arg-beta-2.	Biochim Biophys Acta	1966	0.78
261	Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.	Am J Hematol	1990	0.78
262	The production of haemoglobin C in adult sheep and goats.	Aust J Exp Biol Med Sci	1969	0.78
263	Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron.	Hemoglobin	1989	0.78
264	The structure of goat hemoglobins. II. Structural studies of the alpha chains of the hemoglobins A and B.	J Biol Chem	1968	0.78
265	Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS.	Blood	1976	0.78
266	Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant.	Hemoglobin	1988	0.78
267	Hemoglobin D-beta (0) thalassemia. A case report and family study.	Am J Pediatr Hematol Oncol	1988	0.77
268	Biosynthetic and structural studies of hemoglobin in a patient with congenital dyserythropoietic anemia type I.	Hemoglobin	1977	0.77
269	Hb F-Tokyo or alpha 2G gamma 2 34(B16)Val----Ile, a silent gamma chain variant detected by reverse phase high performance liquid chromatography.	Hemoglobin	1985	0.77
270	Hemoglobin abnormalities in a black family with HB S, hereditary persistence of HB F, and a gamma chain variant; a reevaluation through gene mapping.	Hemoglobin	1984	0.77
271	Alpha-, beta-, and gamma-mRNA levels in beta-thalassemia; transcriptional and translational differences in heterozygotes, homozygotes, and compound heterozygotes.	Hemoglobin	1997	0.77
272	Comparison of the relative quantities of gamma-mRNAs and fetal hemoglobin in SS patients with different haplotypes.	Acta Haematol	1998	0.77
273	Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.	Am J Hematol	1985	0.77
274	Hb-Alberta or alpha2beta2 (101(G3) Glu replaced by Gly), a new high-oxygen-affinity hemoglobin variant causing erythrocytosis.	Hemoglobin	1977	0.77
275	Identification and quantitation of Hb Olympia [beta 20(B2)Val leads to Met] and Hb San Diego [beta 109(G11)Val leads to Met] by high-performance liquid chromatography.	J Chromatogr	1983	0.77
276	Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia.	Hemoglobin	1982	0.77
277	The M gamma chain of human fetal hemoglobin is an A gamma chain with an in vitro modification of gamma 141 leucine to hydroxyleucine.	J Chromatogr	1993	0.77
278	Hemoglobin G Georgia or alpha 2-95 Leu (G-2) beta-2.	Biochim Biophys Acta	1970	0.77
279	Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.	Ann Hematol	1992	0.77
280	An individual with "Miyada"-like hemoglobin indistinguishable from hemoglobin A2.	Biochem Genet	1973	0.77
281	Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.	Hemoglobin	1991	0.77
282	Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene.	Hemoglobin	1990	0.77
283	On the levels of hemoglobins F and A2 in sickle-cell anemia and some related disorders.	Am J Clin Pathol	1974	0.77
284	The separation of human hemoglobin chains by high pressure liquid chromatography.	Prog Clin Biol Res	1981	0.77
285	Some properties of hemoglobin Gun Hill.	Hemoglobin	1977	0.77
286	Analysis of high fetal hemoglobin production in sickle cell anemia patients from the Eastern Province of Saudi Arabia.	Prog Clin Biol Res	1987	0.77
287	Separation of tryptic peptides of normal and abnormal alpha, beta, gamma, and delta hemoglobin chains by high-performance liquid chromatography.	J Chromatogr	1979	0.77
288	Alternate organization of alpha G-Philadelphia globin genes among U.S. black and Italian Caucasian heterozygotes.	Hemoglobin	1984	0.77
289	Hemoglobin Handsworth or alpha2 18(A16)Gly----Arg beta2 in a Saudi newborn.	Hemoglobin	1985	0.77
290	Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant.	Hemoglobin	1991	0.77
291	Hemoglobin Atlanta or alpha 2 beta 2 75 Leu-Pro (E19): an unstable variant found in several members of a Caucasian family.	Biochim Biophys Acta	1975	0.77
292	Differences between the levels of G gamma chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequence.	Biochem Genet	1986	0.77
293	The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations.	Br J Haematol	1994	0.77
294	A Canadian family with Hb Wayne; characterization by HPLC and DNA sequencing.	Hemoglobin	1992	0.77
295	Some notes about Hb Q-India and Hb Q-Iran.	Hemoglobin	1986	0.76
296	The types of hemoglobins and globin chains in hydrops fetalis.	Hemoglobin	1989	0.76
297	Nonallelic structural genes and hemoglobin synthesis.	Hamatol Bluttransfus	1970	0.76
298	Hb Camden and Hb Hope found during routine testing.	Acta Haematol	1975	0.76
299	Two different quadruplicated alpha globin gene arrangements.	Br J Haematol	1987	0.76
300	Hb Chiapas alpha 2 114 Pro replaced by Arg beta 2: identification by high pressure liquid chromatography.	Hemoglobin	1981	0.76
301	Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH).	Hemoglobin	1980	0.76
302	Genetic heterogeneity of beta-thalassemia in southeast Sicily.	Am J Hematol	1995	0.76
303	Hemoglobin Jenkins or hemoglobin-N-Baltimore or alpha-2-beta-2 95Glu.	Biochim Biophys Acta	1966	0.76
304	The human fetal hemoglobins.	Tex Rep Biol Med	1982	0.76
305	The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newborn.	Hemoglobin	1979	0.76
306	Hb Winnipeg or alpha 2 75(EF4)Asp leads to Tyr beta 2 in a large Caucasian family living in Georgia, USA.	Hemoglobin	1983	0.76
307	Hemoglobin Montreal: a new variant with an extended beta chain due to a deletion of Asp, Gly, Leu at positions 73, 74, and 75, and an insertion of Ala, Arg, Cys, Gln at the same location.	Blood	1991	0.76
308	Level of fetal hemoglobin in children with sickle cell anemia: influence of gender, haplotype and alpha-thalassemia-2 trait.	Acta Haematol	1993	0.76
309	Alpha-Thalassemia and fetal hemoglobin.	Blood	1994	0.76
310	The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon ( = arginine) at the 5' end of the second exon.	Br J Haematol	1996	0.76
311	New ultra-micro high-performance liquid chromatographic method for determining the gamma chain composition of hemoglobin F in normal adults.	J Chromatogr	1993	0.76
312	A new beta zero-thalassaemia nonsense mutation (codon 112, T-->A) not associated with a dominant type of thalassaemia in the heterozygote.	Br J Haematol	1993	0.76
313	A new alpha-thalassemia-2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote.	Am J Hematol	1993	0.76
314	Hb Wuming or alpha 2 11(A9)Lys substituting for Gln beta 2.	Hemoglobin	1981	0.76
315	Sheep hemoglobin D, an alpha-chain variant with one apparent amino acid substutution (alpha 15 Gly--Asp).	Biochim Biophys Acta	1968	0.76
316	Hemoglobin Köln in a black: pre- and post-splenectomy red cell survival (DF32P and 51Cr) and the pathogenesis of hemoglobin instability.	Blood	1973	0.76
317	Hb Iowa or alpha 2 beta 2(119)(GH2)Gly----Ala.	Hemoglobin	1990	0.76
318	The G gamma T chain (G gamma 75 Thr; 136 Gly) in Hb F-Charlotte is the product of an A gamma gene with a limited gene conversion and that in Hb F-Waynesboro of a mutated G gamma gene.	Hemoglobin	1995	0.76
319	Molecular characterization of beta-thalassaemia in 174 Greek patients with thalassaemia major.	Br J Haematol	1990	0.76
320	Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient.	Hemoglobin	1989	0.76
321	Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from Tunisia.	Hemoglobin	1992	0.76
322	An individual with Hb-Lepore-Baltimore- delta beta-thalassaemia in a Yugoslavian family.	Scand J Haematol	1976	0.76
323	A chromosome with five gamma-globin genes.	Blood	1988	0.76
324	Haemoglobin Hammersmith precludes monitoring with conventional pulse oximetry.	Can J Anaesth	1994	0.76
325	Hb H disease and mild mental retardation in a black girl with a Hb S heterozygosity.	Hemoglobin	1992	0.75
326	Thalassemia in southern India. Interaction of genes for beta+-, beta o-, and delta o beta o-thalassemia.	Acta Haematol	1980	0.75
327	Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adult.	Hemoglobin	1990	0.75
328	The Atlanta family with hemoglobin Grady revisited.	Am J Hum Genet	1983	0.75
329	Hb P-Nilotic in association with beta0-thalassemia: cis-mutation of a hemoglobin betaA chain regulatory determinant?	J Lab Clin Med	1979	0.75
330	Hemoglobin-Strumica or alpha 2 112(G19) His replaced by Arg beta 2. (With an addendum: hemoglobin-J-Paris-I, alpha 2 12(A10) Ala replaced by Asp beta 2, in the same population).	Biochim Biophys Acta	1975	0.75
331	Incorrect genetic counseling of a couple with beta-thalassemia, due to incomplete testing.	Am J Hum Genet	1993	0.75
332	A note on the inheritance of the hereditary persistence of fetal haemoglobin and the delta-chain variant Hb-A2'.	J Med Genet	1976	0.75
333	Hemoglobin Queens (alpha 34 (B15) Leu replaced by Arg) found in two Chinese families.	Hemoglobin	1982	0.75
334	Hb A2-Babinga, Hb S, and HPFH in members of a family from Creola, Alabama.	Hemoglobin	1984	0.75
335	Hb Lepore Washington-Boston in two Mexican mestizo families.	Rev Invest Clin	1997	0.75
336	Application of high-performance liquid chromatographic methodology to the analysis of hemoglobins synthesized in erythroid progenitor cells.	J Chromatogr	1989	0.75
337	The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia.	Hum Genet	1985	0.75
338	Two rare hemoglobin variants: Hb Pyrgos [beta 83(EF7)Gly-->Asp] and Hb Legnano [alpha 141(Hc3)Arg-->Leu] found in Inner Mongolia, P. R. China.	Hemoglobin	1994	0.75
339	Persistent iron and folate deficiency in a patient with deletional hereditary persistence of fetal hemoglobin; the effect on the relative levels of Hb F and G gamma chains and the corresponding mRNAs.	Hemoglobin	1998	0.75
340	Hb Nunobiki or alpha 2 141 (HC3)Arg-->Cys beta 2 in a Belgian female results from a CGT-->TGT mutation in the alpha 2-globin gene.	Hemoglobin	1996	0.75
341	Construction of two plasmids, each containing three different human globin gene fragments.	Hemoglobin	1987	0.75
342	Post-translational control of human hemoglobin synthesis; the number of alpha chain genes and the synthesis of HB S.	Prog Clin Biol Res	1978	0.75
343	The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population.	Hum Genet	1991	0.75
344	Synthesis of the minor fetal hemoglobin Fic in colonies of erythropoietic precursors isolated from human umbilical cord blood.	Am J Hematol	1982	0.75
345	I. Alteration in the properties of human hemoglobin A by variation in structure: a correlation of structure and function.	CRC Crit Rev Clin Lab Sci	1970	0.75
346	HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black family.	Hemoglobin	1986	0.75
347	Characterization of a newly discovered alpha-thalassaemia-1 in two Spanish patients with Hb H disease.	Br J Haematol	1988	0.75
348	Identification of several alpha-globin gene variations in a small Laotian family.	Acta Haematol	1995	0.75
349	Synthesis of a fixed-length single-stranded DNA probe by blocking primer extension in bacteriophage M13.	Gene	1986	0.75
350	Hemoglobin-Q-India (64 (E13) Asp-His) and beta thalassemia: a case report from Punjab (North India)	Eur J Haematol	1988	0.75
351	Frequency of the alpha-thalassemia-2 gene among Nigerian SS patients and its influence on malaria antibody titers.	Hemoglobin	1993	0.75
352	Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family.	Pediatr Res	1980	0.75
353	Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn.	Hemoglobin	1987	0.75
354	II. Binding of organic phosphates to hemoglobin.	CRC Crit Rev Clin Lab Sci	1970	0.75
355	Haemoglobins D-Los Angeles (alpha2beta2 121 GLU leads to GLN) and J-Baltimore (alpha2beta2 16 GLY leads to ASP) in two Dutch families.	Neth J Med	1975	0.75
356	Hb J-Singa (alpha-78 Asn leads to Asp), a newly discovered hemoglobin variant with the same amino acid substitution as one of the two present in Hb J-Singapore (alpha-78 Asn leads to, alpha-79 Ala leads to Gly).	Biochim Biophys Acta	1984	0.75
357	A newly discovered beta O-thalassemia (IVS-II-850, G-->A) mutation in a north European family.	Hemoglobin	1995	0.75
358	Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada.	Hemoglobin	1985	0.75
359	Variation in clinical severity among patients with Hb Lepore-Boston-beta-thalassaemia is related to the type of beta-thalassaemia.	Br J Haematol	1988	0.75
360	The relative levels of different types of beta-mRNA and beta-globin in BFU-E derived colonies from patients with beta chain variants; further evidence for somatic mosaicism in the Hb Costa Rica carrier [beta 77(EF1)His-->Arg].	Hemoglobin	1996	0.75
361	Isobutyramide therapy in patients with sickle cell anemia.	Am J Hematol	1995	0.75
362	The importance of the 3' untranslated region for the expression of the alpha-globin genes.	Hemoglobin	1996	0.75
363	Two new large deletions resulting in epsilon gamma delta beta-thalassemia.	Acta Haematol	1988	0.75
364	Newer developments in the identification of beta-thalassemia.	Hemoglobin	1988	0.75
365	Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama.	Hemoglobin	1995	0.75
366	Fetal hemoglobin variants identified in adults through restriction endonuclease gene mapping methodology.	Blood	1985	0.75
367	Nucleotide sequence of the human theta 1-globin gene.	Biochem Genet	1988	0.75
368	Hb Leslie is the same as Hb Shelby or alpha 2 beta 2 131 (H9)Gln----Lys.	Hemoglobin	1984	0.75
369	Possible relationship between the level of Hb Bart's (gamma4) and the relative amount of Hb S or Hb C in black heterozygous newborn.	Hemoglobin	1978	0.75
370	alpha-Thalassemia and beta-thalassemia in a Turkish family.	Am J Hematol	1977	0.75
371	Hb F-Austell or alpha 2G gamma (2)40(C6)Arg----Lys.	Hemoglobin	1988	0.75
372	Hb N-Baltimore [alpha 2 beta 2(95)(FG2)Lys----Glu] and Hb J-Iran [alpha 2 beta 2(77)(Ef1]His----Asp] observed in a Turkish family from Antalya.	Hemoglobin	1990	0.75
373	Minor hemoglobins (Hb AI) in chronic alcoholic patients.	Hemoglobin	1982	0.75
374	Hb Gainesville-GA or alpha 2 beta 2 46(CD5)Gly----Arg.	Hemoglobin	1985	0.75
375	Hb Bicêtre or alpha 2 beta(2)63(E7)His----Pro in a white male: clinical observations over a period of 25 years.	Am J Hematol	1986	0.75
376	The characterization of variants of human hemoglobin A2.	Clin Chim Acta	1974	0.75
377	Hb Brockton [alpha 2 beta 2138(H16)Ala----Pro] observed in a Turkish girl.	Hemoglobin	1989	0.75
378	An X-ray determination of the molecular interactions in hemoglobin C: a disease characterized by intraerythrocytic crystals.	Biochem Biophys Res Commun	1979	0.75
379	Hb Oleander, alpha 116(GH4)GLU----GLN, found in a Black female in Georgia.	Hemoglobin	1984	0.75
380	Hemoglobin Beograd or alpha 2 beta 2 121 Glu-Val (GH4).	Biochim Biophys Acta	1973	0.75
381	A second patient with hemoglobin Alberta, a high-oxygen-affinity variant causing erythrocytosis and forming asymmetric tetramers.	Hemoglobin	1978	0.75
382	HB ottawa [alpha 15 (A13) GLY----ARG] found in Hubei Province, People's Republic of China.	J Tongji Med Univ	1986	0.75
383	The hemoglobin P-Galveston-Hb-C conduction in members of a black family from South Carolina.	FEBS Lett	1978	0.75
384	A new slow-moving hemoglobin variant Hb Tianshui or alpha 2 beta(2)39(C5)Gln----Arg, observed in a Chinese family living in Gansu.	Hemoglobin	1990	0.75
385	Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb S.	Hemoglobin	1989	0.75
386	Hb Sögn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosity.	Hemoglobin	1996	0.75
387	The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes.	Blood	1986	0.75
388	The ratio of G gamma and A gamma chains of the hemoglobin F synthesized by BFU-E-derived colonies from blood of subjects with beta+ thalassemia and related hemoglobinopathies.	Ann N Y Acad Sci	1980	0.75
389	Hb F in sickle cell anemia.	Experientia	1993	0.75
390	The M gamma chain of human fetal hemoglobin; its identification and occurrence.	J Chromatogr	1987	0.75
391	Factors associated with hypochromia and microcytosis among high school students in the southeastern United States.	South Med J	1994	0.75
392	Hemoglobin G-San Jose (alpha 2 beta 2 7(A4)Glu replaced by Gly) in a Mexican family.	Hemoglobin	1980	0.75
393	The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes.	Hemoglobin	1986	0.75
394	HB Beth Israel (beta 102 [G4] Asn replaced by Ser) observed in a Yugoslavian teenager.	Hemoglobin	1978	0.75
395	Hb Strasbourg [beta 23(B5)Val-->Asp]; a high oxygen affinity variant observed in a German family.	Hemoglobin	1998	0.75
396	Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln.	Hemoglobin	1990	0.75
397	The determination of the percentages of G gamma and A gamma chains in human fetal hemoglobin by HPLC.	Hemoglobin	1980	0.75
398	Two rare alpha chain variants, Hb Dunn or alpha 26(A4)Asp replaced by Asn beta 2 and Hb G-Pest or alpha 274(EF3)Asp replaced by Asn beta 2, observed in an Indian and a black newborn.	Hemoglobin	1983	0.75
399	Hb Extremadura or alpha 2 beta 2133 (H11)Val----Leu, a new mildly unstable hemoglobin in a Spanish female.	Hemoglobin	1989	0.75
400	Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations.	Acta Haematol	1992	0.75
401	Hb S-Hb Lufkin disease in a black male infant.	Hemoglobin	1995	0.75
402	Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing.	Hemoglobin	1992	0.75
403	The chemical heterogeneity of human hemoglobin F. Direct evidence for the existence of three types of gamma chain, the G gamma I, A gamma I, and A gamma T chains.	Biochim Biophys Acta	1979	0.75
404	Characterization of abnormalities in the gamma-globin gene arrangements of Japanese newborns.	Hemoglobin	1988	0.75
405	Homozygous beta+-thalassemia in a Dutch teenager: haematological, clinical, and genetic observations. A case report.	Neth J Med	1988	0.75
406	Abnormal human haemoglobins in western Kenya.	East Afr Med J	1984	0.75
407	Identification and quantitation of embryonic and three types of fetal hemoglobin produced on induction of the human pluripotent leukemia cell line K-562 with hemin.	Am J Hematol	1982	0.75
408	Haplotype-specific sequence variations in the locus control region (5' hypersensitive sites 2, 3, 4) of beta S chromosomes.	Hemoglobin	1993	0.75
409	Hemoglobin Fort Gordon or alpha2beta2145 Tyr replaced by Asp, a new high-oxygen-affinity hemoglobin variant.	Biochim Biophys Acta	1975	0.75
410	Two different mutations in codon 68 are observed in Hb G-Philadelphia heterozygotes.	Am J Hematol	1994	0.75
411	The distribution of fetal hemoglobin and the types of gamma chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies.	Biochem Med	1983	0.75
412	Hb A2-Manzanares or alpha 2 delta 2 121 (GH4) Glu replaced by Val, an unstable delta chain variant observed in a Spanish family.	Hemoglobin	1983	0.75
413	The role of a sickle cell center in comprehensive screening and counseling for sickle cell and related disorders.	South Med J	1974	0.75
414	Further modification of the microchromatographic determination of hemoglobin A2.	Hemoglobin	1977	0.75
415	Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.	Am J Hematol	1992	0.75
416	Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140.	Biochim Biophys Acta	1988	0.75
417	Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow.	Hemoglobin	1995	0.75
418	Crystallography and oriented single crystal electron microscopy of hemoglobin deer II, a hemoglobin that exhibits matchstick-shaped erythrocytes.	Biochim Biophys Acta	1978	0.75
419	HB Q-Thailand-HB H disease in a Chinese living in Geneva, Switzerland: characterization of the variant and identification of the two alpha-thalassemic chromosomes.	Am J Hematol	1987	0.75
420	Hemoglobin Babinga or alpha 2 delta 2 136 Gly--Asp observed in the American Negro.	Biochim Biophys Acta	1969	0.75
421	Association of the level of G gamma chain in the fetal hemoglobin of normal adults with specific haplotypes.	Hemoglobin	1986	0.75
422	Probable inclusion-body beta-thalassemia in a Chinese family.	Hemoglobin	1977	0.75
423	Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg].	Hemoglobin	1988	0.75
424	Hb A2-liangcheng [delta 117(G19)Asn->Asp(AAC->GAC)]: a new delta chain variant detected by gene analysis in a Chinese family.	Hemoglobin	1993	0.75
425	Hemoglobinopathies affecting maternal-fetal oxygen gradient during pregnancy: molecular, biochemical and clinical studies.	Am J Perinatol	1998	0.75
426	Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys in a Spanish family.	Hemoglobin	1987	0.75
427	Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese family.	Hemoglobin	1989	0.75
428	Characterization of three types of beta zero-thalassemia resulting from a partial deletion of the beta-globin gene.	Hemoglobin	1989	0.75
429	Abnormal gamma-globin gene arrangements in Sardinians.	Hemoglobin	1988	0.75
430	The usefulness of sequence analysis of amplified DNA for the identification of delta chain variants.	Hemoglobin	1991	0.75
431	Structural studies of hemoglobin chains from Virginia white-tailed deer.	Arch Biochem Biophys	1972	0.75
432	A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication.	Ann Hematol	1991	0.75
433	Hemoglobin Louisville (beta 42 (CD1) phenylalanine replaced by leucine) occurring as a fresh mutation in a Canadian woman.	Hemoglobin	1978	0.75
434	Sickle cell anemia identified in a multiple-transfused patient through analysis of mRNA with an RT-PCR-based technique.	Acta Haematol	1995	0.75
435	Some physicochemical properties of hemoglobin-manitoba (alpha2 102Ser replaced by Arg (G9) beta2).	Biochim Biophys Acta	1975	0.75
436	Hemoglobin Athens-Georgia, or alpha 2 beta 2 40(C6)Arg replaced by Lys, a hemoglobin variant with an increased oxygen affinity.	Biochim Biophys Acta	1976	0.75
437	Thalassemia intermedia in two patients with Hb Lepore-beta zero-thalassemia (Frameshift codon 8, -AA).	Hemoglobin	1994	0.75
438	HB Mizuho or alpha 2 beta 2 68(E12)Leu-->Pro in a young Dutch boy.	Hemoglobin	1995	0.75
439	Hb F-Columbus-Ga or alpha 2 G gamma 2 94(FGl) Asp replaced by Asn.	Hemoglobin	1982	0.75
440	On the structure of the hemoglobins A, A2, and F in a Negro with homozygous beta-thalassemia.	Biochem Med	1974	0.75
441	The polymorphism of human fetal hemoglobin.	Birth Defects Orig Artic Ser	1982	0.75
442	Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation.	Acta Haematol	1994	0.75
443	An improved chromatographic procedure for quantitation of human fetal hemoglobin.	Hemoglobin	1977	0.75
444	An elongated segment of DNA observed between two human alpha globin genes.	Hum Genet	1986	0.75
445	Structural aspects of fetal and adult hemoglobins from nonanemic ruminants.	Ann N Y Acad Sci	1974	0.75
446	A second family with the Atlanta type of HPFH.	Hemoglobin	1985	0.75
447	The primary sequence of the beta chain of Hb type III of the Virginia white-tailed deer (Odocoilus Virginianus), a comparison with putative sequences of the beta chains from four additional deer hemoglobins, types II, IV, V, and VIII, and relationships between intermolecular contacts, primary sequence and sickling of deer hemoglobins.	Hemoglobin	1983	0.75
448	Two delta-chain abnormal hemoglobins in one individual.	Blood	1965	0.75
449	Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn.	Hemoglobin	1990	0.75
450	[Molecular characterization of a Spanish family with alpha-thalassemia].	Rev Clin Esp	1988	0.75
451	Heterogeneity of gamma-globin chain synthesis in Saudi newborns.	Int J Hematol	1991	0.75
452	Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatography.	Hemoglobin	1993	0.75
453	Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermedia.	Am J Hematol	1995	0.75
454	Hb Nottingham (alpha2beta2 (FG5) 98 val leads to gly) in a Caucasian male: clinical and biosynthetic studies.	Hemoglobin	1978	0.75
455	Biochemical and molecular aspects of beta-thalassemia types in northern Sardinia.	Hemoglobin	1988	0.75
456	Hb Savaria or alpha(2)49(CE7)Ser----Arg beta 2 in a Yugoslavian family.	Hemoglobin	1985	0.75
457	Hb Sassari or alpha (2)126(H9)Asp---His beta 2 observed in a family from Northern Sardinia.	Hemoglobin	1987	0.75
458	Production of hemoglobin C in the Moufflon (Ovis musimon Pallas, 1811) and the Barbary sheep (Ammotragus lervia Pallas, 1777) during experimental anemia: amino acid composition of tryptic peptides from the beta B and bet C chains.	Biochem Genet	1970	0.75
459	Hemoglobinopathies observed in the population of the Southeastern United States (SE-USA).	Hemoglobin	1980	0.75
460	DNA polymorphisms in North Sardinian newborns and their linkage with abnormal gamma globin gene arrangements and with beta (0) -thalassemia.	Biochem Genet	1986	0.75
461	The identification of five rare beta-chain abnormal hemoglobins by high performance liquid chromatographic procedures.	Hemoglobin	1986	0.75
462	Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female.	Hemoglobin	1987	0.75
463	The Greek A gamma beta+-HPFH observed in a large black family.	Am J Hematol	1987	0.75
464	Hb Camperdown or alpha 2 beta 2(104)(G6)Arg----Ser in two Italian males.	Hemoglobin	1990	0.75
465	An IVS-I-117 (G-->A) acceptor splice site mutation in the alpha 1-globin gene is a nondeletional alpha-thalassaemia-2 determinant in an Indian population.	Br J Haematol	1993	0.75
466	Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia.	Am J Hematol	1994	0.75
467	Adult hemoglobin levels in newborn babies from different countries and in babies with some significant hemoglobinopathies.	Acta Haematol	1987	0.75
468	Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses.	J Chromatogr	1991	0.75
469	Hb Madrid or alpha 2 beta (2)115(G17)Ala-->Pro in a black teenager.	Hemoglobin	1993	0.75
470	Application of high pressure liquid chromatography and microsequencing methodology in the structural analysis of human hemoglobin variants.	Sci Sin B	1983	0.75
471	Oxygen equilibrium analyses of isolated hemoglobins A2, Lepore-Washington and P-nilotic.	Biochim Biophys Acta	1978	0.75
472	The frequencies of Hbs S and C in Georgia and South Carolina.	Hum Genet	1991	0.75
473	Chromatographic methods for the separation of normal and abnormal hemoglobins.	Hemoglobin	1980	0.75
474	Hb A2-Grovetown or alpha 2 delta (2)75(E19)Leu-->Val.	Hemoglobin	1993	0.75
475	Hb Doha or alpha 2 beta 2[X-N-Met-1(NA1)Val----Glu]; a new beta-chain abnormal hemoglobin observed in a Qatari female.	Biochim Biophys Acta	1985	0.75
476	Hemoglobin Alamo (alpha2beta2 19 (b1) Asn replaced by Asp).	Hemoglobin	1977	0.75
477	Hb Cheverly or alpha 2 beta 2 45(CD4)Phe replaced by Ser in an elderly Italian male.	Hemoglobin	1982	0.75
478	Hb F-Sacromonte or alpha 2G gamma (2)59(E3)Lys-->Gln observed in a Spanish newborn and his mother.	Hemoglobin	1993	0.75
479	Observations on the calculated contents of variant and normal alpha chains in adult and fetal erythrocytes.	Hemoglobin	1979	0.75
480	Gamma-chain heterogeneity of fetal hemoglobin in nonblack beta- and delta beta- thalassemia and HPFH heterozygotes and homozygotes.	Am J Hematol	1982	0.75
481	Hb F-Auckland [alpha 2G gamma 2(7)(A4)Asp----Asn] observed in a Caucasian newborn from Alabama.	Hemoglobin	1985	0.75
482	Hemoglobin Hamilton or alpha 2 beta 2 11(A8)Val leads to Ile: a silent beta-chain variant detected by Triton X-100 acid-urea polyacrylamide gel electrophoresis.	Am J Hematol	1984	0.75
483	Hb G-Taipei or beta 22(B4)Glu----Gly in a Chinese family living in The Netherlands.	Hemoglobin	1987	0.75
484	Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly.	Hemoglobin	1985	0.75
485	Hb F-Jiangsu, the first gamma chain variant with a valine----methionine substitution: alpha 2A gamma 2 134(H12)Val----Met.	Hemoglobin	1990	0.75
486	Hb Lepore-Baltimore (delta 68Leu-beta 84Thr) and Hb Lepore-Washington-Boston (delta 87Gln-beta IVS-II-8) in central Portugal and Spanish Alta Extremadura.	Hum Genet	1997	0.75
487	Microchromatographic quantitation of fetal hemoglobin in patients with sickle cell disease.	Hemoglobin	1979	0.75
488	Hemoglobin Kariya or alpha 240(C5)Lys----Glu beta 2 in a Caucasian family from South Carolina.	Hemoglobin	1984	0.75
489	Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys.	Hemoglobin	1987	0.75
490	Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes.	Hemoglobin	1990	0.75
491	Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia.	Hemoglobin	1993	0.75
492	HB G-Copenhagen or alpha 2 beta 2(47) (CD6) Asp----Asn observed in a black newborn.	Hemoglobin	1985	0.75
493	Hb G-Szuhu or alpha 2 beta 2(80)(EF4)Asn----Lys, in combination with beta zero-thalassemia in a Spanish family.	Hemoglobin	1985	0.75
494	Hb F-Xin-Su or A gamma I73(E17)Asp----His: a new slow-moving fetal hemoglobin variant.	Hemoglobin	1987	0.75
495	Gene duplication of the alpha chain of goat hemoglobin: evidence from a homozygous mutant.	Biochim Biophys Acta	1968	0.75
496	Hb F-Veleta or alpha 2 G gamma(2)40(C6)Arg-->Gly.	Hemoglobin	1995	0.75
497	Transient chloramphenicol acetyltransferase expression of the G gamma globin gene 5'-flanking regions containing substitutions of C----T at position -158, G----A at position -161, and T----A at position -175 in K562 cells.	Biochim Biophys Acta	1989	0.75
498	The effect of pH on the uptake of methylene blue by human red cells.	Clin Chim Acta	1970	0.75
499	Beta-thalassemia intermedia in an Indian female with the Hb Hofu [beta 126(H4)Val-->Glu]-beta zero-thalassemia [codons 8/9 (+G)] combination.	Hemoglobin	1995	0.75
500	A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease.	Am J Hematol	1992	0.75
501	Hb Capa or alpha (2)94(G1)Asp-->Gly beta 2, a mildly unstable variant with an A-->G (GAC-->GGC) mutation in codon 94 of the alpha 1-globin gene.	Hemoglobin	1994	0.75
502	Peripheral haemolysis, lipid peroxidation, iron status, and vitamin E in haemoglobin H syndromes in West Malaysia.	Singapore Med J	1993	0.75
503	Hb Davenport or alpha 2(78)(EF7)Asn----His beta 2.	Hemoglobin	1990	0.75
504	The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia.	Biochim Biophys Acta	1996	0.75
505	Beta zero-thalassemia in association with a gamma-globin gene quadruplication.	Blood	1986	0.75
506	In vitro synthesis of hemoglobin and hemoglobin chains in the BFUe-derived colonies form person with alpha- or beta-thalassemia.	Am J Hematol	1981	0.75
507	Long survival in sickle cell anemia.	Trop Geogr Med	1975	0.75
508	Hemoglobin Riyadh-beta 0-thalassemia in an Indian family.	Hemoglobin	1979	0.75
509	The thalassemia syndromes in association with hemoglobinopathies in southern China.	Hemoglobin	1988	0.75
510	Hemoglobin Chapel Hill or alpha2 74 Asp replaced by Gly beta2.	FEBS Lett	1976	0.75
511	[Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].	Vnitr Lek	1993	0.75
512	Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican families.	Hemoglobin	1981	0.75
513	Hb F-Kennestone or alpha 2G gamma 2 (EF1)77 His leads to Arg observed in a Caucasian baby.	Hemoglobin	1983	0.75
514	The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed.	Hum Genet	1994	0.75
515	Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp).	Hemoglobin	1994	0.75
516	Saudi Arabian sickle cell anemia. A molecular approach.	Ann N Y Acad Sci	1989	0.75
517	Hemoglobins A 2 -Sphakiá and A 2 -NYU in Canada.	Can J Biochem	1972	0.75
518	Structure of human hemoglobin C: a disease with intraerythrocytic crystals.	Biochim Biophys Acta	1979	0.75
519	[Hemoglobin F Catalonia. A new variant of fetal hemoglobin].	Sangre (Barc)	1991	0.75
520	Hb Nottingham or alpha 2 beta 2(98)(FG5)Val----Gly observed as a de novo mutation in a Canadian child.	Hemoglobin	1992	0.75
521	Hb F-Bonaire-Ga or alpha 2 A gamma 2 39(C5) Gln replaced by Arg, characterized by high pressure liquid chromatographic and microsequencing procedures.	Hemoglobin	1982	0.75
522	Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family.	Hemoglobin	1985	0.75
523	The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemia.	Hemoglobin	1982	0.75
524	The structure of sheep hemoglobins. 3. Structural studies on the alpha chain of hemoglobin A.	J Biol Chem	1968	0.75
525	Hb F-Charlotte, an A gamma variant with a threonine residue in position gamma 75 and a glycine residue in position gamma 136.	Hemoglobin	1990	0.75
526	Hb Sabine or alpha 2 beta 2 91 (F7) Leu----Pro in a Yugoslavian boy.	Hemoglobin	1983	0.75
527	The structure of goat hemoglobins. V. A fourth beta chain variant (beta-D-Malta; 69 Asp is replaced by Gly) with decreased oxygen affinity and occurring at a high frequency in Malta.	Hemoglobin	1979	0.75
528	Hb Cordele alpha(2)47 (CE5)Asp----Ala beta 2. A mildly unstable variant observed in black twins.	Hemoglobin	1984	0.75
529	Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2.	Hemoglobin	1992	0.75
530	Haemoglobin M Saskatoon and haemoglobin M Hyde Park in two Yugoslavian families.	Scand J Haematol	1974	0.75
531	Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNA.	Biochim Biophys Acta	1989	0.75
532	Hb Suresnes or alpha2 141(HC3) ArgyieldHis beta2 in a black family.	Hemoglobin	1978	0.75
533	An unusual phenotypic expression of Hb-Leiden.	Biochem Genet	1982	0.75
534	Hb F-Saskatoon or alpha 2G gamma (2)21(B3)Glu-->Lys observed in a North American Indian newborn.	Hemoglobin	1993	0.75
535	Low quantities of Hb Boyle Heights or alpha 2(6)(A4)Asp----O beta 2 observed in three members of a Caucasian family.	Hemoglobin	1990	0.75
536	Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report.	Hemoglobin	1989	0.75
537	Hb Mizuho or alpha 2 beta (2)68(E12)Leu----Pro in a Caucasian boy with high levels of Hb F; identification by sequencing of amplified DNA.	Hemoglobin	1991	0.75
538	Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant.	Hemoglobin	1987	0.75
539	Hemoglobin F levels in patients with chronic renal failure.	Hemoglobin	1977	0.75
540	Unstable Hb Newcastle [beta92(F8)His-->Pro], first case discovered in a Russian patient.	Hemoglobin	1999	0.75
541	Identification of the alpha chain abnormal hemoglobin Jackson (alpha 127 Lys leads to Asn) after isolation of the core peptide by high-performance liquid chromatography.	J Chromatogr	1983	0.75
542	A comparison of two procedures useful for the isolation of Hb F from adult red blood cells and for the quantitation of the types of gamma chain by high-performance liquid chromatography.	J Chromatogr	1984	0.75
543	Molecular heterogeneity of beta-thalassemia intermedia in Turkey.	Acta Haematol	1989	0.75
544	Hb F-Catalonia or alpha 2G gamma(2)15(A12)Trp----Arg.	Hemoglobin	1990	0.75
545	Letter: Hereditary persistence of foetal haemoglobin.	Nature	1975	0.75
546	Thalassemia intermedia caused by heterozygosity for both beta-thalassemia and hemoglobin Saki [beta 14 (A11) Leu replaced by Pro].	Am J Hematol	1976	0.75
547	Hb F-Meinohama or alpha 2 gamma 2 (5 Glu replaced by Gly; 75 Ile; 136 Gly).	Hemoglobin	1981	0.75
548	The beta zero-thalassemia in an American black family is due to a single nucleotide substitution in the acceptor splice junction of the second intervening sequence.	Am J Hematol	1986	0.75
549	Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNA.	Hemoglobin	1995	0.75
550	Hemoglobin Hofu or alpha 2 beta 2 [126 (H4) Va1 leads to Glu] found in combination with hemoglobin S.	Hemoglobin	1978	0.75
551	Haemoglobin Presbyterian [beta 108 (G 10) Asn----Lys] in a Spanish family.	Acta Haematol	1986	0.75
552	Homozygosity for hemoglobin O-Arab (alpha 2 beta 2 121 Glu----Lys). Hb O-Arab disease.	Turk J Pediatr	1986	0.75
553	A second observation of Hb Abruzzo [alpha 2 beta 2(143)(H21)His----Arg] in an Italian family.	Hemoglobin	1990	0.75
554	Hemoglobin S-Ga Georgia disease: a case report.	Acta Haematol	1974	0.75
555	Genetic aspects of gamma chain synthesis.	Hamatol Bluttransfus	1972	0.75
556	Hb Savaria or alpha2 (49)(CE7)Ser----Arg beta2 in an indigenous female from Kenya.	Hemoglobin	1985	0.75
557	Hb D-Granada or alpha 2 beta 2 22(B4)Glu----Val.	Hemoglobin	1987	0.75
558	Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb A.	Br J Haematol	1988	0.75
559	The frequency of the A gamma T gene in the presence and absence of the beta S or beta C gene in the Black population of the Southeastern USA.	Hemoglobin	1981	0.75
560	Heterogeneity of fetal hemoglobin among Israel families with beta-thalassemia.	Isr J Med Sci	1974	0.75
561	The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA.	Hemoglobin	1992	0.75
562	A second, elongated, alpha 2-globin mRNA is present in reticulocytes from normal persons and subjects with terminating codon or poly A mutations.	Biochem Biophys Res Commun	1995	0.75
563	Hb Fukuyama or alpha 2 beta(2)77(EF1)His----Tyr observed in an Indonesian female.	Hemoglobin	1991	0.75
564	Hb A2-Zagreb or alpha 2 delta 2(125)(H3)Gln replaced by Glu, a new delta chain variant in association with delta beta-thalassemia.	Hemoglobin	1983	0.75
565	The first homozygote for the hereditary persistence of fetal hemoglobin observed in the southeastern United States.	Hemoglobin	1981	0.75
566	[Haplotype in 3 patients homozygous for beta-thalassemia].	Sangre (Barc)	1987	0.75
567	Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).	Biochem Genet	1992	0.75
568	Hb F-Marietta or G gamma I 80[EF4] Asp replaced by Asn, observed in a Caucasian baby.	Hemoglobin	1982	0.75
569	An Indonesian family with the Southeast Asian type of alpha-thalassemia-1 and a gamma-globin gene triplication.	Acta Haematol	1987	0.75
570	Postnatal changes in the quantities of globin chains and hemoglobin types in two babies with Hb H disease.	Am J Hematol	1993	0.75
571	Two hemoglobin phenotypes in the American bison (Bison bison): a possible genetic explanation based on structural studies.	Biochem Genet	1973	0.75
572	Percentages of abnormal hemoglobins in adults with a heterozygosity for an alpha-chain and/or a beta-chain variant.	Am J Hematol	1983	0.75
573	Hb-Genova ( 2 2 28(B10)Leu leads to Pro ); methods for detection and analysis of unstable hemoglobins.	Clin Chim Acta	1973	0.75
574	Hb Zengcheng or alpha 2 beta(2)114(G16)Leu----Met.	Hemoglobin	1990	0.75
575	Hb Köln or alpha 2 beta 2(98)(FG5)Val----Met in a Czechoslovakian family.	Hemoglobin	1991	0.75
576	Hb Hradec Kralove (Hb HK) or alpha 2 beta 2 115(G17)Ala-->Asp, a severely unstable hemoglobin variant resulting in a dominant beta-thalassemia trait in a Czech family.	Hemoglobin	1993	0.75
577	beta S-haplotypes and alpha-thalassemia along the coastal belt of Kenya.	East Afr Med J	1989	0.75
578	The gamma chain heterogeneity of fetal hemoglobin in black beta-thalassemia and HPFH heterozygotes.	Blood	1981	0.75
579	Three sickle cell anemia patients each with a different alpha chain variant. Diagnostic complications.	Hemoglobin	1993	0.75
580	A new delta chain variant, haemoglobin-A2-Melbourne or alpha2 delta2 43Glu-Lys(CD2).	Biochim Biophys Acta	1974	0.75
581	Hb Chapel Hill or alpha 274(EF3)Asp----Gly beta 2 observed in a Chinese family in association with beta-thalassemia.	Hemoglobin	1986	0.75
582	[Preferential synthesis of fetal hemoglobin in in vitro cultures of erythroid precursors from peripheral blood of healthy persons and those with hemoglobinopathies].	Bilt Hematol Transfuz	1979	0.75
583	Hb J-Pontoise or alpha 2(63)(E12)Ala----Asp beta 2 in four members of a Spanish family.	Hemoglobin	1987	0.75
584	Fetal hemoglobin heterogeneity in Chinese newborns of the Uygur and Han nationalities; comparisons of babies from Xinjiang and Beijing.	Hemoglobin	1987	0.75
585	Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification.	Biochim Biophys Acta	1986	0.75
586	Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time.	Hemoglobin	1989	0.75
587	A newly discovered frameshift at codons 120-121 (+A) of the beta gene is not associated with a dominant form of beta-thalassemia.	Blood	1996	0.75
588	Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb Rampa.	J Lab Clin Med	1978	0.75
589	Zeta and theta 1-globin gene deletions located on the same chromosome.	Br J Haematol	1989	0.75
590	Hb Lepore-Baltimore in a north Sardinian family.	Hemoglobin	1990	0.75
591	A second observation of Hb F-Lodz or alpha 2G gamma (2)44(CD3)Ser----Arg.	Hemoglobin	1991	0.75
592	Separation of the A gamma and G gamma cyanogen bromide peptides of human fetal hemoglobin by high-pressure liquid chromatography.	Anal Biochem	1979	0.75
593	Hb Regina or alpha 2 beta 2 96(FG3)Leu----Val: a high oxygen affinity variant discovered by cation-exchange HPLC.	Am J Hematol	1985	0.75
594	Viscosity and gelation studies in deer hunting hemoglobins.	Proc Soc Exp Biol Med	1975	0.75
595	A second family with Hb Minneapolis-Laos or alpha 2 beta (2)118(GH1)Phe----Tyr.	Hemoglobin	1987	0.75
596	Is the trimodality of Hb Leslie (alpha 2 beta 2 131 Gln---O) in heterozygotes the result of a variable number of active alpha-chain genes? Evidence for posttranslational control of hemoglobin synthesis.	Am J Hematol	1978	0.75
597	Hb-Volga or alpha 2 beta 2 27(B9)Ala replaced by Asp. An unstable hemoglobin variant in three generations of a Dutch family.	Biochim Biophys Acta	1976	0.75
598	Hb Rainier or alpha 2 beta 2 (145 (HC2) Tyr replaced by Cys) observed in members of a Canadian family of Greek origin.	Hemoglobin	1979	0.75
599	MRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variants.	Am J Hematol	1996	0.75
600	Historical note: the beta-thalassemia allele in the noble Russian family Lermontov is identified as the ATG-->ACG change in the initiation codon.	Hemoglobin	1998	0.75
601	Haemoglobin alpha chain duplication in Barbary sheep, Ammotragus lervia, Pallas, 1777.	Nature	1970	0.75
602	Detection of the alpha-thalassemia-2 (3.7 kb) deletion in DNA extracted from 20-year-old blood smears.	Hemoglobin	1997	0.75
603	A new gamma chain variant: Hb F-Pordenone [gamma 6(A3) Glu replaced by Gln: 75ILE: 136ALA].	Hemoglobin	1982	0.75
604	A mutation associated with elevated G gamma chain in sickle cell anemia and hereditary persistence of fetal hemoglobin.	Prog Clin Biol Res	1985	0.75
605	Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant.	Biochim Biophys Acta	1982	0.75
606	3. Hemoglobin heterogeneity and structural genes.	CRC Crit Rev Clin Lab Sci	1970	0.75
607	Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.	Hemoglobin	1988	0.75
608	The combination of HB S and HB E in a black female.	Hemoglobin	1977	0.75
609	Hb F-Calluna or alpha 2 gamma 2(12 Thr replaced by Arg; 75Ile; 136Ala) in a Caucasian baby.	Hemoglobin	1983	0.75
610	Hb Ramona or alpha (2)24(B5)Tyr-->Cys beta 2.	Hemoglobin	1994	0.75
611	Further evidence for non-linkage of the Hb and Hb structural loci in man.	Clin Chim Acta	1972	0.75
612	The quantities of various minor hemoglobin components in old and young human red blood cells.	Clin Chim Acta	1967	0.75
613	Hb Bushwick [beta 74(E18)Gly----Val] heterozygotes in a Yugoslavian family have 35 to 40% of the unstable variant.	Hemoglobin	1987	0.75
614	Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus.	Hemoglobin	1983	0.75
615	Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian family.	Hemoglobin	1989	0.75
616	A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.	Hemoglobin	1991	0.75
617	Globin mRNA in beta-thalassemia heterozygotes with different beta-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin.	Acta Haematol	1996	0.75
618	Hemoglobin types in Barbary sheep (Ammotragus lervia Pallas, 1777); absence of a betaC production in a homozygous beta C(na) animal during severe anemia.	Proc Soc Exp Biol Med	1972	0.75
619	Hb Albany-GA or alpha 2(11)(A9)Lys leads to Asn beta 2.	Hemoglobin	1983	0.75
620	Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.	Hemoglobin	1987	0.75
621	Hb Beograd (alpha2 beta2 121 (GH4) Glu replaced by Val) observed in a new Yugoslavian family.	Hemoglobin	1978	0.75
622	Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family.	Hemoglobin	1991	0.75
623	Hemoglobin Hacettepe or alpha 2 beta 2 127 (H5) Gln replaced by Glu.	Biochim Biophys Acta	1976	0.75
624	Synthesis of hemoglobin chains in adult and newborn goats: possible influence of the beta c synthesis on the production of alpha chains.	Hemoglobin	1982	0.75
625	Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia allele.	Acta Haematol	1990	0.75
626	Alpha-thalassemia and the production of different alpha chain variants in heterozygotes.	Biochem Genet	1981	0.75
627	Relative levels of alpha-, beta-, and gamma-mRNA from patients with severe and intermediate beta-thalassemia major.	Acta Haematol	1997	0.75
628	Studies on the heterogeneity of hemoglobin. XVI. Separation of variants with a GlU-Lys substitution by chromatography on CM-cellulose.	J Chromatogr	1974	0.75
629	Chemical heterogeneity of foetal haemoglobin in the Lepore haemoglobinopathy.	Br J Haematol	1974	0.75
630	Hb Beograd-beta zero thalassemia in a Turkish family from Yugoslavia.	Hemoglobin	1984	0.75
631	[Homozygote beta-thalassemia in 2 Dutch families].	Ned Tijdschr Geneeskd	1989	0.75
632	Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia trait.	Am J Hematol	1994	0.75
633	Oxygen equilibria and biochemical changes of whole blood stored in different preservation media.	Transfusion	1969	0.75
634	Identical nucleotide sequences of the 3'A gamma globin gene enhancer elements from four different chromosomes.	Blood	1989	0.75
635	Hb Guangzhou-Hangzhou or alpha 2(64)(E13)Asp----Gly beta 2 observed in members of a Chinese family living in Xinjiang.	Hemoglobin	1990	0.75
636	The structure of goat hemoglobins. 3. Hemoglobin D, a beta chain variant with one apparet amino acid substitution (21 Asp--His).	Arch Biochem Biophys	1968	0.75
637	Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish family.	Hemoglobin	1987	0.75
638	Hb F-Forest Park, a new A gamma variant with two amino acid substitutions, 75(E19)Ile----Thr and 73(E17)Asp----Asn, which can be identified in adults by gene-mapping analysis.	Biochim Biophys Acta	1985	0.75
639	Further studies on the quantitation of the hemoglobins A, S, C, and F in newborn babies with different hemoglobinopathies using high pressure liquid chromatography.	Hemoglobin	1982	0.75
640	Detection of a new hybrid alpha 2 globin gene among American blacks.	Hum Genet	1988	0.75
641	Carboxymethyl-cellulose microchromatography for the quantitation of hemoglobin Bart's (gamma 4) and its use in the detection of the alpha-thalassemia conditions.	J Chromatogr	1980	0.75
642	Restriction endonuclease gene mapping studies of an Indian (A gamma delta beta)zero-thalassaemia, previously identified as G gamma-HPFH.	Br J Haematol	1984	0.75
643	Hb Volga or alpha 2 beta 2 27(B9)Ala----Asp in an Italian family.	Hemoglobin	1985	0.75
644	Hb Cleveland or alpha 2 beta 2(93)(F9)Cys----Arg;121(GH4)Glu----Gln.	Hemoglobin	1991	0.75
645	[Structural variants in hemoglobin occurring in the Czech Republic].	Vnitr Lek	1995	0.75
646	Effect of severe hemorrhage on the hemoglobins of a Virginian white-tailed deer (Odocoileus virginianus).	Proc Soc Exp Biol Med	1968	0.75
647	Distribution of beta-thalassemia mutations in three Asian Indian populations with distant geographical locations.	Hemoglobin	1994	0.75
648	[Hemoglobin Complutense (beta 127 (H5) Gln replaced by Glu) in a Spanish family].	Sangre (Barc)	1987	0.75
649	Hb Porto Alegre or alpha 2 beta 29(A6)Ser->Cys in unrelated families of the Canary Islands.	Hemoglobin	1993	0.75
650	The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes.	Experientia	1994	0.75
651	Co-inheritance of Hb D-Punjab (codon 121; GAA-->CAA) and beta (0) -thalassemia (IVS-II-1;G-->A).	J Pediatr Hematol Oncol	1996	0.75
652	Construction of three plasmids, each containing two or three different human globin gene fragments.	Hemoglobin	1988	0.75
653	Hb Brockton [alpha 2 beta 2(138)(H16)Ala-->Pro] observed in a Spanish girl.	Hemoglobin	1992	0.75
654	Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography.	J Chromatogr	1989	0.75
655	Hb Etobicoke, alpha 85(F5) Ser leads to Arg found in a newborn of French-Indian-English descent.	Hemoglobin	1983	0.75
656	Posttranslational modification of beta 141 Leu associated with the beta 75(E19)Leu-->Pro mutation in Hb Atlanta.	Hemoglobin	1993	0.75
657	Geographic distribution of hemoglobin variants in the white-tailed deer.	J Mammal	1973	0.75
658	Hb F-Albaicin or G gamma 8(A5)Lys----Glu or Gln.	Hemoglobin	1986	0.75
659	Hb F-Beech Island or alpha 2A gamma 2(53)(D4)Ala----Asp.	Hemoglobin	1985	0.75
660	Detection of the embryonic zeta chain in blood from newborn babies by reversed-phase high-performance liquid chromatography.	J Chromatogr	1987	0.75
661	Hb F-Pendergrass, an A gamma I variant with a Pro----Arg substitution at position gamma 36(C2).	Hemoglobin	1985	0.75

T H Huisman

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