Published in Int J Cancer on September 30, 1993
The Human Y Chromosome: The Biological Role of a "Functional Wasteland" J Biomed Biotechnol (2001) 0.88
A database for human Y chromosome protein data. Bioinformation (2009) 0.75
Y-chromosome status identification suggests a recipient origin of posttransplant non-small cell lung carcinomas: chromogenic in situ hybridization analysis. Hum Pathol (2014) 0.75
Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome. N Engl J Med (1969) 2.19
A randomized study of high-dose cytarabine in induction in acute myeloid leukemia. Blood (1996) 2.06
Fluorodeoxyuridine synchronization of bone marrow cultures. Cancer Genet Cytogenet (1983) 1.22
Familial polycythaemia vera: a study of 3 sisters. Scand J Haematol (1976) 1.16
Plasma cell membrane glycoprotein PC-1. cDNA cloning of the human molecule, amino acid sequence, and chromosomal location. J Biol Chem (1990) 1.14
Lymphoblastic leukemia with marked eosinophilia: a report of two cases. Blood (1973) 1.13
X-linkage of human phosphoglycerate kinase confirmed in man-mouse and man-Chinese hamster somatic cell hybrids. Am J Hum Genet (1971) 1.13
Chromosomal abnormalities identify high-risk and low-risk patients with acute lymphoblastic leukemia. Blood (1986) 1.12
Mosaicism for trisomy 17-18 and trisomy 13-15 in man. Nature (1965) 1.11
Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups. J Med Genet (1969) 1.09
Numerical abnormalities of the X chromosome. Frequency among inpatients of a general hospital and in a general population. Lancet (1966) 1.00
Cytogenetic features of twenty-six primary breast cancers. Cancer Genet Cytogenet (1991) 0.95
Human adenosine deaminase and chromosome 20. Experientia (1978) 0.93
The presence of mast cells in agar cultures. Exp Hematol (1980) 0.92
Interleukin-5 is at 5q31 and is deleted in the 5q- syndrome. Blood (1988) 0.91
Functional evidence for a colorectal cancer tumor suppressor gene at chromosome 8p22-23 by monochromosome transfer. Cancer Res (1996) 0.91
Multiple congenital skin webbing with cutis laxa. Br J Plast Surg (1970) 0.89
Fourth International Workshop on Chromosomes in Leukemia 1982: Translocation (8;21)(q22;q22) in acute nonlymphocytic leukemia. Cancer Genet Cytogenet (1984) 0.89
Cellular and karyotypic characterization of two doxorubicin resistant cell lines isolated from the same parental human leukemia cell line. Int J Cancer (1994) 0.89
Platelet-phosphohexokinase levels in Down's syndrome. Lancet (1968) 0.89
Long-term survival of patients with acute myeloid leukemia: a third follow-up of the Fourth International Workshop on Chromosomes in Leukemia. Cancer (1997) 0.89
Six-year follow-up of the clinical significance of karyotype in acute lymphoblastic leukemia. Cancer Genet Cytogenet (1989) 0.87
Localization of the G-CSF gene on chromosome 17 proximal to the breakpoint in the t(15;17) in acute promyelocytic leukemia. Blood (1987) 0.87
Molecular deletion of 9p sequences in non-small cell lung cancer and malignant mesothelioma. Genes Chromosomes Cancer (1993) 0.85
Clinicopathological characteristics of acute lymphoblastic leukemia with the 4;11 chromosome translocation. Pathology (1984) 0.84
Acute leukaemia associated with an abnormal genotype. Scand J Haematol (1974) 0.83
Long-term survival in acute myelogenous leukemia: a second follow-up of the Fourth International Workshop on Chromosomes in Leukemia. Cancer Genet Cytogenet (1994) 0.83
Chromosome 16 abnormalities associated with myeloid malignancies. Genes Chromosomes Cancer (1991) 0.82
Rearrangement of chromosome 1p in breast cancer correlates with poor prognostic features. Br J Cancer (1992) 0.82
A collaborative study of the relationship of the morphological type of acute nonlymphocytic leukemia with patient age and karyotype. Blood (1982) 0.81
Cytogenetic analysis of 147 cases of non-Hodgkin's lymphoma: non-random chromosomal abnormalities and histological correlations. Br J Haematol (1990) 0.81
New translocation t(2;13)(p12;q34) and rearrangement of the MLL gene in a childhood leukemia cell line. Genes Chromosomes Cancer (1995) 0.81
Chromosome abnormalities in non-small cell lung cancer pleural effusions: cytogenetic indicators of disease subgroups. Genes Chromosomes Cancer (1993) 0.81
Constitutive heterochromatin (C-banding) studies in patients with testicular malignancies. Cancer Genet Cytogenet (1981) 0.81
Direct evidence for involvement of erythroid cells in acute myeloblastic leukaemia. Lancet (1974) 0.81
Two malignant peripheral primitive neuroepithelial tumor cell lines established from consecutive samples of one patient: characterization and cytogenetic analysis. Genes Chromosomes Cancer (1992) 0.81
Chromosomal localization of amplified N-myc in neuroblastoma cells using a biotinylated probe. Cancer Genet Cytogenet (1992) 0.80
Patterns of failure with increasing intensification of induction chemotherapy for acute myeloid leukaemia. Br J Haematol (2001) 0.80
Acute non-lymphocytic leukaemia. Clin Haematol (1980) 0.79
Breast cancer cytogenetics and beyond. Aust N Z J Surg (1990) 0.79
Hybrid biphenotypic acute leukemia with extreme hypodiploidy. Pathology (1987) 0.79
The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders. Leukemia (1994) 0.79
A girl with Wolf-Hirschorn syndrome and mosaicism 46,XX-46,XX,4p-. J Ment Defic Res (1974) 0.78
Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphocytic leukemia. Cancer Genet Cytogenet (1988) 0.78
t(1;3)(p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic-clinicopathologic association. Blood (1985) 0.78
Prospective study of childhood acute lymphocytic leukemia: hematologic, immunologic, and cytogenetic correlations. Med Pediatr Oncol (1988) 0.78
Atypical Duffy blood group inheritance and chromosome abnormalities. Nature (1965) 0.78
The 45, XO, Ph 1 subgroup of chronic granulocytic leukaemia. Scand J Haematol (1972) 0.78
3. The value of chromosome studies in the classification and management of the leukemias. Pathology (1982) 0.77
Characterization of homogeneously staining regions in a small cell lung cancer cell line, using in situ hybridization with an MYCN probe. Genes Chromosomes Cancer (1994) 0.77
Detection of MYCN amplification in three neuroblastoma cell lines by non-radioactive chromosomal in situ hybridization. Cancer Genet Cytogenet (1992) 0.77
Acute nonlymphocytic leukemia after transient myeloproliferative disorder in a patient with Down syndrome. Med Pediatr Oncol (1990) 0.77
Characterization of a new human bladder cancer cell line, UCRU-BL-28. J Urol (1993) 0.77
Characterization of cell lines derived from a multiply aneuploid human bladder transitional-cell carcinoma, UCRU-BL-13. Int J Cancer (1989) 0.77
Cytogenetics of acute lymphoblastic leukaemia in children as a factor in the prediction of long-term survival. Br J Haematol (1982) 0.77
Clinical findings in patients with numerical abnormalities of the X chromosome: a three-year survey of consecutive admissions to a general hospital. Med J Aust (1980) 0.77
Two cases of de novo precursor B-cell acute lymphoblastic leukemia with t(14;18), but without cytogenetic evidence of an associated Burkitt's or Burkitt's variant translocation. Am J Clin Pathol (1994) 0.76
Down's Syndrome with translocation-en-tandem: a report of two unrelated cases. Aust Paediatr J (1970) 0.76
Establishment and characterization of a childhood pre-B acute lymphoblastic leukemia cell line, PER-278, with chromosome translocations t(1;19) and t(1;9). Cancer Genet Cytogenet (1990) 0.76
Studies in a patient with acute leukaemia after lysergide treatment. Br Med J (1969) 0.76
Chromosomal findings in acute lymphoblastic leukaemia of childhood: an independent prognostic factor. Lancet (1981) 0.76
A complicated but nonrandom karyotype in preleukemia. Cancer Genet Cytogenet (1984) 0.76
Inheritance of chromosome 7 is associated with a drug-resistant phenotype in somatic cell hybrids. Br J Cancer (1996) 0.75
The influence of colcemid concentration on mitotic index and length of bone marrow chromosomes. Pathology (1983) 0.75
Localization of the cell surface antigen CD7 by chromosomal in situ hybridization. Immunogenetics (1990) 0.75
Fourth International Workshop on Chromosomes in Leukemia 1982: Chromosomes in acute promyelocytic leukemia. Cancer Genet Cytogenet (1984) 0.75
Treatment of acute promyelocytic leukaemia relapsing after allogeneic bone marrow transplantation with all-trans-retinoic acid: suppression of the leukaemic clone. Br J Haematol (1991) 0.75
Assignment of the gene coding for human FcRII (CD32) to bands q23q24 on chromosome 1. Immunogenetics (1988) 0.75
Eosinophilic leukemia or reactive eosinophilia? Cancer Genet Cytogenet (1984) 0.75
t(14;18) in a case of diffuse lymphoma. N Engl J Med (1983) 0.75
Chronic granulocytic leukemia: correlation of blastic transformation type with karyotypic evolution. Am J Hematol (1985) 0.75
Immunoglobulin allotypes Gm and Km in hematologic malignancies. Cancer Genet Cytogenet (1988) 0.75
Fc receptor gene translocation in a t(1;19) pre-B ALL cell line. Immunogenetics (1990) 0.75
Chromosome abnormalities in leukaemia and lymphoma. Ann Acad Med Singapore (1984) 0.75
The multiple basal cell nevus syndrome: a cytogenetic study of six cases. Cancer Genet Cytogenet (1986) 0.75
A review of the t(1;19) breakpoints in acute lymphocytic leukemia. Cancer Genet Cytogenet (1985) 0.75
Trisomy 4 in acute nonlymphocytic leukemia. An Australian case. Cancer Genet Cytogenet (1988) 0.75
A simple G-banding technique following nonradioactive in situ hybridization. Cytogenet Cell Genet (1993) 0.75
The proportion of erythroid mitoses in normal human bone marrow in short-term culture systems. Pathology (1989) 0.75
Acute lymphoblastic leukemia with a hypodiploid karyotype with less than 40 chromosomes: the basis for division into two subgroups. Leukemia (1989) 0.75
Erythroblastic transformation of chronic granulocytic leukemia: a clinical and cytogenetic case study. Am J Hematol (1983) 0.75
Cytogenetic abnormalities in lung cancer. Cancer Treat Res (1989) 0.75
The value of bone marrow cell synchronization. Cancer Genet Cytogenet (1984) 0.75
Sequential karyotypes in non-Hodgkin lymphoma: their nature and significance. Genes Chromosomes Cancer (1990) 0.75
Chromosome studies in inherited nonpolyposis colon cancer syndrome. Cancer Genet Cytogenet (1987) 0.75
Novel translocation (2;4) with consistent involvement of 2p23 in acute nonlymphocytic leukemia (M2). Cancer Genet Cytogenet (1992) 0.75
The human FCG1 gene encoding the high-affinity Fc gamma RI maps to chromosome 1q21. Immunogenetics (1993) 0.75
The human metallothionein gene cluster is not disrupted in myelomonocytic leukemia. Genomics (1990) 0.75
Regional localization of the gene for clusterin (SP-40,40; gene symbol CLI) to human chromosome 8p12-->p21. Cytogenet Cell Genet (1992) 0.75
Translocation 1;19--a new cytogenetic abnormality in acute lymphocytic leukemia. Cancer Genet Cytogenet (1984) 0.75
Double 9;22 translocation with hyperdiploidy appearing in blastic transformation of chronic granulocytic leukemia. Cancer Genet Cytogenet (1982) 0.75
Silver bands in chronic granulocytic leukemia: I. Increased banding associated with blastic transformation. Cancer Genet Cytogenet (1984) 0.75