Published in Lancet on October 25, 1975
Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement. J Med Genet (1979) 1.31
Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens. J Clin Invest (1994) 1.15
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia. J Clin Invest (1994) 0.90
Pericentric inversions of human chromosomes 9 and 10. Am J Hum Genet (1974) 2.40
Xg and sex-chromosome abnormalities. Br Med Bull (1969) 2.06
Clearance of Rh D-positive red cells with monoclonal anti-D. Lancet (1990) 2.04
Failure to detect linkage between Xg and other X-borne loci in Sardinians. Ann Hum Genet (1966) 1.82
Failure to demonstrate linkage between the loci for the Rh and Duffy blood groups. Ann Hum Genet (1973) 1.81
Evidence that the Xg locus is inactivated in structurally abnormal X chromosomes. Nature (1970) 1.58
Xg groups and sex abnormalities in people of northern European ancestry. J Med Genet (1971) 1.56
The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups. Ann Hum Genet (1969) 1.52
Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum. J Med Genet (1977) 1.32
The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus. Am J Hum Genet (1965) 1.31
An inherited X-autosome translocation in man. Ann Hum Genet (1971) 1.30
[48, XXXX syndrome in a six year old child. Abnormal transmission of group Xg]. Ann Genet (1968) 1.26
New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups. J Med Genet (1974) 1.24
Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis. Ann Hum Genet (1969) 1.23
Antigenic and structural analysis of Treponema denticola. J Gen Microbiol (1989) 1.17
8-Trisomy in the bone marrow. Report of two cases. Clin Genet (1972) 1.16
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation. Lancet (1970) 1.13
Chromosome pulverization in blood diseases. Hereditas (1981) 1.10
[Radioimmunoassay of alpha-fetoprotein in primary and secondary cancer of the liver]. J Natl Cancer Inst (1972) 1.08
The linkage relation of Xg to g-6-pd in Israelis: the evidence of a second series of families. Ann Hum Genet (1967) 1.08
The X-linked blood group system Xg tests on British, Northern American, and northern European unrelated people and families. J Med Genet (1966) 1.08
X g and X chromosome inactivation. Lancet (1971) 1.06
Red cell antigen, serum protein and red cell enzyme polymorphisms in Karkar Islanders and inhabitants of the adjacent North Coast of New Guinea. Hum Hered (1982) 1.05
Xg blood-groups and clonal-origin theory of chronic myeloid leukaemia. Lancet (1970) 1.04
Linkage studies in X-linked retinitis pigmentosa. Humangenetik (1972) 1.04
Ocular albinism and Xg. Lancet (1968) 1.02
Decrease of the major high molecular weight surface glycoprotein of human granulocytes in monosomy-7 associated with defective chemotaxis. Blood (1979) 1.01
Abnormalities of chromosome No. 17 in myeloproliferative disorders. Cancer Genet Cytogenet (1982) 0.99
Inheritance of testicular feminization syndrome: some negative linkage findings. J Med Genet (1969) 0.98
Ocular albinism and Xg. Lancet (1971) 0.98
The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry. J Med Genet (1971) 0.97
Studies of carcino-fetal proteins. II. Biochemical comparison of -fetoprotein from human fetuses and patients with hepatocellular cancer. Int J Cancer (1971) 0.97
Alpha-fetoprotein and hepatitis B antigen in acute hepatitis and primary cancer of the liver. Scand J Gastroenterol (1973) 0.97
Hemolytic anemia and thrombocytopenia in a case of left atrial myxoma associated with mitral stenosis. Am J Cardiol (1966) 0.96
X-linked cataract. Ann Hum Genet (1967) 0.95
Function of neutrophils in preleukaemia. Scand J Haematol (1977) 0.95
Glycophorin A as a cell surface marker of early erythroid differentiation in acute leukemia. Int J Cancer (1979) 0.95
An Allele of the S(s) Blood Group Genes. Proc Natl Acad Sci U S A (1954) 0.94
The red cell phenotype En(a-) and anti-Ena: serological and physicochemical aspects. Vox Sang (1969) 0.94
Agranulocytosis in patients treated with clozapine. A study of the Finnish epidemic. Acta Psychiatr Scand (1977) 0.93
Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents. J Med Genet (1968) 0.92
Mk and Mg: some serological and physicochemical observations. Vox Sang (1969) 0.90
Persistent mixed field polyagglutinability. Electrokinetic and serological aspects. Vox Sang (1971) 0.89
X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred. Ann Hum Genet (1969) 0.89
Red cell antigen, serum protein and red cell enzyme polymorphisms in Eastern Highlanders of New Guinea. Hum Hered (1982) 0.89
Bone lesions in chronic myelogenous leukaemia. Acta Med Scand (1981) 0.88
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases. Hum Genet (1982) 0.88
Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus. J Med Genet (1973) 0.87
Source of single X in XO Turner syndrome: a comment. Hum Genet (1985) 0.87
Anomalous Xg inheritance with a probable explanation. Lancet (1971) 0.87
The 5q- chromosome in preleukaemia and acute leukaemia. Scand J Haematol (1981) 0.86
X-linked retinitis pigmentosa and linkage studies with the Xg blood-groups. Lancet (1967) 0.86
Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy. Hum Genet (1983) 0.86
Antigens Aua, i and P1 of cells of the dominant type of Lu(a-b-). Vox Sang (1974) 0.86
Haema synthesis during pyridoxine therapy in two families with different types of hereditary sideroblastic anaemia. Ann Clin Res (1982) 0.85
The Colton blood groups in monosomy 7 of the bone marrow. Birth Defects Orig Artic Ser (1976) 0.85
Erythroid blast crisis in chronic myelogenous leukemia. Blood (1983) 0.85
Trisomy 8 in the bone marrow associated with high red cell glutathione reductase activity. Blood (1976) 0.85
Defective neutrophil migration in monosomy-7. Blood (1981) 0.84
Chromosome changes in human chronic lymphocytic leukemia. Cancer Genet Cytogenet (1981) 0.84
Some contributions of blood groups to human genetics. Am J Clin Pathol (1971) 0.84
Impaired neutrophil chemotaxis in Pelger-Huët anomaly. Clin Exp Immunol (1979) 0.84
Blood group mosaics. Haematologia (Budap) (1972) 0.83
Fisher's contribution to Rh. Vox Sang (1982) 0.83
Five cases of positive antiglobulin test involving IgA warm type autoantibody. Ann Clin Res (1971) 0.82
A new antibody, anti-Fy3, in the Duffy blood group system. Vox Sang (1971) 0.82
Polyploidy of the bone marrow. Scand J Haematol (1976) 0.82
Structures of Miltenberger class I and II specific major human erythrocyte membrane sialoglycoproteins. Eur J Biochem (1984) 0.81
Plant agglutinin for another human blood-group. Lancet (1971) 0.81
The effect of naturally occurring Rh antibodies on the survival of serologically incompatible red cells. Br J Haematol (1987) 0.81
Serology and genetics of an MNSs-associated antigen Dantu. Vox Sang (1984) 0.81
Glucocorticoid receptors and glucocorticoid sensitivity of human leukemic cells. Int J Cancer (1980) 0.80
Platelet function in preleukaemia. Scand J Haematol (1981) 0.80
Phenotypically normal individuals with an inversion (X) (p22q13) and the recombinant (X), dup q. Ann Hum Genet (1981) 0.80
Cell surface glycoprotein analysis: a diagnostic tool in human leukemias. Int J Cancer (1979) 0.80
Culture of bone marrow reveals more cells with chromosomal abnormalities than the direct method in patients with hematologic disorders. Blood (1981) 0.79
Circulating haematopoietic progenitors in myelofibrosis. Scand J Haematol (1982) 0.79
Expression of blood group A antigens in human bone marrow cells. Blood (1981) 0.79
XI. The hereditary blood factors of the Kurds of Iran. Philos Trans R Soc Lond B Biol Sci (1973) 0.79
Gerbich blood group system: a useful genetic marker in certain Melanesians of Papua and New Guinea. Nature (1970) 0.79
Coumarin anticogulant requirement in relation to serum cholesterol and triglyceride level. Acta Med Scand (1968) 0.79
The blood group antigen Ula (Karhula). Vox Sang (1968) 0.78
Red cell antigen, serum protein, and red cell enzyme polymorphisms in inhabitants of the Jimi Valley, Western Highlands, New Guinea. Hum Genet (1981) 0.78
An inhibitor of chemotaxis and phagocytosis in reticulum cell sarcoma. Scand J Haematol (1975) 0.78
Increased sister chromatid exchange in megaloblastic anaemia-studies on bone marrow cells and lymphocytes. Hereditas (1978) 0.78
Early fusion of two human embryos? Ann Hum Genet (1974) 0.78
Effect of long-term training and acute physical exercise on red cell 2,3-diphosphoglycerate. Eur J Appl Physiol Occup Physiol (1979) 0.78
Glucocorticoid receptors in hairy-cell leukemia. Int J Cancer (1982) 0.77
Acute erythroleukaemia with L3 morphology and the 14q+ chromosome. Scand J Haematol (1982) 0.77
Blood groups of the Irish. Ann Hum Biol (1977) 0.77
Sister chromatid exchanges in human bone marrow cells. I. Control subjects and patients with leukaemia. Hereditas (1978) 0.77
Haem biosynthesis in refractory sideroblastic anaemia associated with the preleukaemic syndrome. Scand J Haematol (1981) 0.77
Red cell glucose-6-phosphate dehydrogenase deficiency in Finland. Characterization of a new variant with severe enzyme deficiency. Scand J Haematol (1975) 0.77
Effect of short-term treatment with an anabolic steroid (methandienone) and dehydroepiandrosterone sulphate on plasma hormones, red cell volume and 2,3-diphosphoglycerate in athletes. Scand J Clin Lab Invest (1977) 0.77
The Dombrock system: linkage relations with other blood group loci. J Med Genet (1972) 0.76