Published in Am J Hum Genet on September 01, 1966
A special role of the group 17,18 chromosomes in reticuloendothelial neoplasia. Br J Cancer (1970) 1.09
The role of genetic diversity in cancer. J Clin Invest (2010) 1.05
Agar culture and chromosome analysis of eosinophilic leukaemia. J Clin Pathol (1975) 0.96
Cytogenetic evolution and clonal proliferation in acute transformation of chronic granulocytic leukaemia. Br J Cancer (1968) 0.95
Chromosome studies in tumours and leukemia. Can Med Assoc J (1990) 0.75
Clonal evolution in two patients with autoimmune disease and lymphoreticular neoplasia. Br J Cancer (1970) 0.75
Chromosome studies on normal and leukemic human leukocytes. J Natl Cancer Inst (1960) 4.15
Nucleolus-organisers in the causation of chromosomal anomalies in man. Lancet (1961) 3.55
Cytogenetic studies in chronic myeloid leukaemia and acute leukaemia associated with monogolism. Lancet (1961) 2.73
Persistent chromosome aberrations in irradiated human subjects. Radiat Res (1962) 1.78
Cytogenetic studies on bone-marrow in chronic myeloid leukaemia. Lancet (1963) 1.77
CHROMOSOME STUDIES DURING EARLY AND TERMINAL CHRONIC MYELOID LEUKAEMIA. Br Med J (1964) 1.57
Chronic granulocytic leukemia of childhood. Clinical and cytogenetic studies. J Pediatr (1963) 1.53
CHROMOSOMAL DIFFERENCES AMONG THE ACUTE LEUKEMIAS. Ann N Y Acad Sci (1964) 1.45
Comparison of chromosome constitution in chronic myelocytic leukemia and other myeloproliferative disorders. Blood (1962) 1.31
CHRONIC GRANULOCYTIC LEUKAEMIA. THE CHROMOSOMES AND THE DISEASE. Lancet (1964) 1.26
[MICROTECHNIC FOR THE STUDY OF HUMAN CHROMOSOMES FROM A HUMAN LEUKOCYTE CULTURE]. Ann Genet (1964) 1.12
Chronic granulocytic leukemia and the Philadelphia chromosome. Blood (1963) 1.09
Chromosomal alteration of erythropoietic cells in chronic myeloid leukemia. Acta Haematol (1963) 1.06
[Chromosome analyses in idiopathic acquired sideroblastic anemia. A study of 6 cases]. Nouv Rev Fr Hematol (1967) 1.06
MULTIPLE CHROMOSOMAL ABNORMALITIES IN AN ACUTE EXACERBATION OF MYELOID LEUKAEMIA. Lancet (1965) 1.04
IN VIVO EFFECTS OF DIAGNOSTIC X-IRRADIATION ON HUMAN CHROMOSOMES. N Engl J Med (1964) 1.02
Philadelphia chromosome in eosinophilic leukemia. Am J Med (1965) 1.00
CYTOGENETIC EVIDENCE OF CLONAL PROLIFERATION IN PRIMARY RETICULAR NEOPLASMS. Proc Can Cancer Conf (1963) 0.99
TWO LEUKEMIC PERIPHERAL BLOOD STEMLINES DURING ACUTE TRANSFORMATION OF CHRONIC MYELOGENOUS LEUKEMIA IN A D/D TRANSLOCATION CARRIER. Cytogenetics (1965) 0.94
A new chromosome abnormality in chronic granulocytic leukaemia. Br Med J (1961) 0.90
BLASTIC CRISIS IN CHRONIC GRANULOCYTIC LEUKAEMIA. CYTOCHEMICAL, CYTOGENETIC, AND AUTORADIOGRAPHIC STUDIES IN FOUR CASES. Br Med J (1964) 0.89
CHROMOSOME STUDIES IN LEUKEMIA. I. EVIDENCE FOR THE ORIGIN OF LEUKEMIC STEM LINES FROM ANEUPLOID MUTANTS. N Engl J Med (1964) 0.89
BLOOD AND SKIN CHROMOSOMAL ALTERATIONS OF A CLONAL TYPE IN A LEUKEMIC MAN PREVIOUSLY IRRADIATED FOR A LUNG CARCINOMA. Cytogenetics (1964) 0.86
SUBMETACENTRIC CHROMOSOME IN CHRONIC MYELOCYTIC LEUKEMIA. Arch Intern Med (1964) 0.85
CYTOGENETIC STUDIES IN CHRONIC MYELOID LEUKEMIA. Adv Cancer Res (1963) 0.84
TWO CASES OF CHRONIC MYELOID LEUKAEMIA WITH PRESUMABLY IDENTICAL 47-CHROMOSOME CELL-LINES IN THE BLOOD. Acta Pathol Microbiol Scand (1964) 0.83
Double Ph 1 chromosomes in leukaemia. Lancet (1966) 0.83
Two Ph1 chromosomes in acute granulocytic leukaemia. A study of two cases. Lancet (1965) 0.82
[ Chromosome analysis of a clonal development in a case of myeloid leykemia]. Nouv Rev Fr Hematol (1966) 0.82
[2 cases of acute myeloblastic leukemia with normal and haploid (21 or 22) blood cells]. Rev Fr Etud Clin Biol (1963) 0.81
PRESENCE OF TWO PH-1 CHROMOSOMES IN CELLS FROM A PATIENT WITH CHRONIC GRANULOCYTIC LEUKAEMIA. Nature (1965) 0.80
PH1-positive chronic myelogenous leukemia, with absence of another G chromosome, in a male. N Engl J Med (1965) 0.80
A case of chronic myeloid leukaemia with a 45-chromosome cell-line in the blood. Cytogenetics (1962) 0.80
[PH CHROMOSOME AND 5-12 TRANSLOCATION IN A CASE OF CHRONIC MYELOID LEUKEMIA]. Rev Clin Esp (1964) 0.78
[CHROMOSOMAL ANALYSIS OF CANCER CELLS AND OF MEDULLARY AND BLOOD CELLS IRRADIATED "IN VITRO"]. Ann Genet (1963) 0.77
UNTREATED CHRONIC MYELOCYTIC LEUKEMIA ASSOCIATED WITH AN UNUSUAL CHROMOSOME PATTERN. Ann Intern Med (1964) 0.77
DEVELOPMENT AND POSSIBLE SIGNIFICANCE OF ABNORMAL CELL-LINES IN THE ACUTE STAGE OF CHRONIC MYELOGENOUS LEUKAEMIA. Scand J Haematol (1965) 0.77
CHROMOSOMES IN ALEUKAEMIC LEUKAEMIA. Lancet (1965) 0.77
[Chromosomes and human leukemias. The concept of clonal development]. Ann Genet (1965) 0.77
[Study of chromosomes in 35 cases of leukemia]. Presse Med (1966) 0.77
SEVERAL CELL-LINES WITH ABNORMAL KARYOTYPES IN A PATIENT WITH CHRONIC MYELOGENOUS LEUKAEMIA. Scand J Haematol (1964) 0.77
[HAPLOSOMY 21 ASSOCIATED WITH A TRISOMY 6-12 IN A TUBERCULOTIC PRESENTING A BLOOD AND MEDULLARY MYELOBLASTOSIS]. Nouv Rev Fr Hematol (1965) 0.77
X-RAYS AND PHILADELPHIA CHROMOSOME. Lancet (1965) 0.76
[Chromosome development of chronic myeloid leukemia]. Ann Genet (1965) 0.76
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature (1990) 2.80
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nat Genet (1992) 1.76
Beta amyloid gene duplication in Alzheimer's disease and karyotypically normal Down syndrome. Science (1987) 1.67
Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34. Hum Genet (1976) 1.63
Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin). Ann Genet (1984) 1.62
[Intercalary deletions of 9q]. Ann Genet (1978) 1.58
[5-21-22 translocation and the crying cat syndrome]. Ann Genet (1965) 1.50
Partial trisomy 9q: a new syndrome. Humangenetik (1975) 1.46
Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases. Hum Genet (1984) 1.42
[2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q]. Ann Genet (1972) 1.38
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex. Ann Genet (1980) 1.34
[48, XXXX syndrome in a six year old child. Abnormal transmission of group Xg]. Ann Genet (1968) 1.26
[46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child]. Ann Genet (1968) 1.20
De novo del(3)(q2800). Ann Genet (1984) 1.20
[Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+]. Ann Genet (1971) 1.18
Familial t(X;2) (p223;q323) with partial trisomy 2q and male and female balanced carriers. Hum Genet (1977) 1.17
Distal trisomy 17q. Clin Genet (1979) 1.12
Chromosomal abnormalities and congenital heart disease. Circulation (1967) 1.12
Trisomy 22q12 leads to qter: "aneusomie de recombinaison" of a pericentric inversion. Ann Genet (1981) 1.11
Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism. Hum Genet (1987) 1.09
[Distal 14q trisomy]. Ann Genet (1983) 1.09
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1. Hum Genet (1986) 1.09
X-linked hypohidrotic ectodermal dysplasia and t(X;12) in a female. Clin Genet (1989) 1.09
T-lymphocyte colonies in the lymphoproliferative disorders. Immunology (1978) 1.09
Are clinical and biological IVF parameters correlated with chromosomal disorders in early life: a multicentric study. Hum Reprod (1988) 1.08
Acute renal failure following collective intoxication by Cortinarius orellanus. Intensive Care Med (1990) 1.07
[Chromosome analyses in idiopathic acquired sideroblastic anemia. A study of 6 cases]. Nouv Rev Fr Hematol (1967) 1.06
Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D. Hum Genet (1981) 1.04
Trisomy 18q-. Trisomy mapping of chromosome 18 revisited. Clin Genet (1980) 1.03
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11. Hum Genet (1988) 1.02
Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3). Ann Genet (1982) 1.01
Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band. Humangenetik (1974) 1.00
[Fibroblasts in culture during mucopolysaccharidoses: the effect of serum on metachromasy]. Ann Genet (1968) 1.00
Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric region. Ann Genet (1985) 1.00
[Mosaic trisomy 14 due to an iso dicentric chromosome (author's transl)]. Ann Genet (1980) 0.99
Parental origin of the extra chromosomes in polysomy X. Hum Genet (1994) 0.99
[21 p-maternal in duplicate in a case of trisomy 21]. Ann Genet (1970) 0.99
Del11p13/nephroblastoma without aniridia. Hum Genet (1984) 0.99
Inherited hypertrichoses. Clin Genet (2002) 0.98
A complex familial chromosome translocation. Am J Hum Genet (1965) 0.98
[6-12 13-15 translocation and partial 6-12 trisomy (probably 10)]. Ann Genet (1965) 0.97
[Partial 7 q trisomy. One or 2 syndromes? Apropos of a new case]. Ann Genet (1976) 0.97
Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23. Hum Genet (1982) 0.97
Cytogenetic forms of retinoblastoma: their incidence in a survey of 66 patients. Cancer Genet Cytogenet (1985) 0.96
[De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child]. Ann Genet (1974) 0.96
[Distal trisomy 15q]. Ann Genet (1977) 0.96
Trisomy 18qter and trisomy mapping of chromosome 18. Clin Genet (1977) 0.96
White blood cell transfusions. Isr J Med Sci (1965) 0.96
[Polyploidisation and clonal evolutions]. Ann Genet (1969) 0.95
[Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation]. Ann Genet (1969) 0.95
Antisera to selected outer membrane proteins of Vibrio cholerae protect against challenge with homologous and heterologous strains of V. cholerae. FEMS Immunol Med Microbiol (1998) 0.95
[Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)]. Ann Genet (1970) 0.95
Trisomy 6qter. Clin Genet (1981) 0.95
[Coagulation factor VII deficiency in 3 patients with trisomy 8]. Ann Genet (1974) 0.94
[F fing chromosome (46, XY, Fr) in a boy with multiple abnormalities]. Ann Genet (1972) 0.93
Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome). Hum Genet (1987) 0.93
Autosomal dominant inheritance in adiposis dolorosa (Dercum's disease). Humangenetik (1973) 0.93
[Chromosomal studies from cell cultures. Technical modifications]. Ann Genet (1970) 0.93
Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma. Hum Genet (1989) 0.93
[Localization of the gene for ribulose-5-phosphate-3-epimerase on the 2q32 to 2qter segment by interspecies cellular hybridization]. Ann Genet (1982) 0.93
[Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family]. Ann Genet (1966) 0.92
[Demonstration of the fine structure of human chromosomes by enzymatic digestion (especially pronase)]. C R Acad Sci Hebd Seances Acad Sci D (1971) 0.92
[Fetomaternal transfusion of blood lymphocytes and identification of the sex of the fetus]. Ann Genet (1971) 0.91
Aneusomie de recombinaison: three further examples. Am J Hum Genet (1966) 0.91
[Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3]. Ann Genet (1974) 0.91
Cytogenetic analysis and developmental capacity of normal and abnormal embryos after IVF. Hum Reprod (1989) 0.90
Monosomy 10qter. Hum Genet (1979) 0.90
[Chromosome anomalies in generalized scleroderma. A study of 6 patients]. C R Acad Sci Hebd Seances Acad Sci D (1969) 0.90
Chromosome investigations in early life. II. Human preimplantation embryos. Hum Reprod (1987) 0.90
Chromosome analysis of human oocytes and embryos: does delayed fertilization increase chromosome imbalance? Hum Reprod (1988) 0.89
Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature. Clin Genet (1984) 0.88
[Waldenstrôm's macroglobulinemia. Developmental and prognostic study]. Sem Hop (1975) 0.88
[Triploid (69, XXX) child having lived for 9 days]. Ann Genet (1974) 0.88
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies. Am J Med Genet (1989) 0.88
6q1 monosomy: a distinctive syndrome. Clin Genet (1988) 0.88
[Regional localization of the genes for human IDHs, MDHs PGK, alphaGAL, G6PD by interspecific hybridization (author's transl)]. Hum Genet (1977) 0.88
Prediction of the response to chemotherapy in acute leukemia. Cancer (1975) 0.87
[Monosomy 7qter (author's transl)]. Ann Genet (1979) 0.87
Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X. Am J Med Genet (1990) 0.87
Embryonic testicular regression syndrome and severe mental retardation in sibs. Ann Genet (1985) 0.87
Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation. Ann Genet (1980) 0.87
Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy. Ann Genet (1985) 0.86
Genetic diseases, chromosome rearrangements, and malignancy. Ann Intern Med (1966) 0.86
Physical map around the retinoblastoma gene: possible genomic imprinting suggested by NruI digestion. Genomics (1991) 0.86
[Subacute myelo-monocytic leukemia. Study of 27 cases and review of the literature]. Sem Hop (1972) 0.85
[Excess of males in trisomy 21 (author's transl)]. Ann Genet (1979) 0.85
Normal human bone marrow cultures in vitro: cellular composition and maturation of the granulocytic colonies. Br J Haematol (1977) 0.85
Molecular detection of constitutional deletions in patients with retinoblastoma. Am J Med Genet (1991) 0.85
[Comparative karyotyping of our gibbon species or subspecies (author's transl)]. Ann Genet (1982) 0.85
[In vitro effect of antibiotics against hospital strains of Acinetobacter baumanii]. Pathol Biol (Paris) (1989) 0.85
Panel of twenty-five independent man-rodent hybrids for human genetic marker mapping. Ann Genet (1986) 0.84
[Extracardiac malformations associated with congenital cardiopathies (statistical study of 1000 cases)]. Acta Genet Med Gemellol (Roma) (1967) 0.84
Discordance for giant pigmented nevi in monozygotic twins. Ann Genet (1973) 0.84