Published in Science on April 10, 1970
Asynchronous replication of heterochromatin in maize. Proc Natl Acad Sci U S A (1980) 1.68
Is Drosophila dAT on the Y chromosome? Proc Natl Acad Sci U S A (1971) 1.32
Novel properties of satellite DNA from muskmelon. Proc Natl Acad Sci U S A (1974) 1.15
Repeated DNA sequences in the heterochromatic Y chromosome of adult Drosophila melanogaster. Proc Natl Acad Sci U S A (1973) 0.89
A family of three related satellite DNAs in Drosophila virilis. Proc Natl Acad Sci U S A (1973) 0.84
Satellite DNA sequence content of polylysine-titratable and nuclease-resistant fractions of mouse liver hepatoma chromatin. Nucleic Acids Res (1976) 0.81
Satellite DNA induces unstable expression of the adjacent herpes simplex virus tk gene cotransfected in mouse cells. Mol Cell Biol (1988) 0.79
High resolution of human chromosomes. Science (1976) 5.56
The chromosomal basis of human neoplasia. Science (1983) 4.26
The origin of man: a chromosomal pictorial legacy. Science (1982) 4.02
Distinctive chromosomal abnormalities in histologic subtypes of non-Hodgkin's lymphoma. N Engl J Med (1982) 3.82
Constitutive fragile sites and cancer. Science (1984) 3.30
Retinoblastoma and subband deletion of chromosome 13. Am J Dis Child (1978) 3.11
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. Science (1980) 2.72
Multiple recurrent genomic defects in follicular lymphoma. A possible model for cancer. N Engl J Med (1987) 1.94
New chromosome techniques in the study of human neoplasia. Hum Pathol (1981) 1.82
The characterization of high-resolution G-banded chromosomes of man. Chromosoma (1978) 1.79
Mid-prophase human chromosomes. The attainment of 2000 bands. Hum Genet (1981) 1.79
A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes. Cytogenet Cell Genet (1978) 1.75
A simple G-banding technique. Lancet (1973) 1.72
Heterochromatin, satellite DNA, and cell function. Structural DNA of eucaryotes may support and protect genes and aid in speciation. Science (1971) 1.67
High-resolution chromosome analysis in clinical medicine. Prog Clin Pathol (1978) 1.64
Ascitic fluid adenosine deaminase insensitivity in detecting tuberculous peritonitis in the United States. Hepatology (1996) 1.39
New chromosomal syndromes. Am J Dis Child (1975) 1.39
Cloning, expression and localization of an RNA helicase gene from a human lymphoid cell line with chromosomal breakpoint 11q23.3. Nucleic Acids Res (1992) 1.38
All patients with acute nonlymphocytic leukemia may have a chromosomal defect. N Engl J Med (1981) 1.29
Characterization of banding patterns of metaphase-prophase G-banded chromosomes and their use in gene mapping. Cytogenet Cell Genet (1978) 1.26
Localization of sequences specifying messenger RNA to light-staining G-bands of human chromosomes. Chromosoma (1977) 1.24
Trisomy 9 mosaicism. Clin Genet (1977) 1.22
Partial trisomy 8 (8q24) and the trisomy-8 syndrome. Humangenetik (1974) 1.22
Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes. Blood (1986) 1.20
Congenital asymmetry associated with trisomy 18 mosaicism. Am J Dis Child (1965) 1.18
Localization of mouse satellite DNA in constitutive heterochromatin. Exp Cell Res (1970) 1.15
Trisomy for the distal segment of chromosome 13: a new syndrome. Am J Dis Child (1974) 1.14
The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee. Science (1980) 1.14
Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13. Humangenetik (1974) 1.14
Serial serum creatine phosphokinase MB isoenzyme activity after myocardial infarction. Studies in the baboon and man. Circulation (1977) 1.11
Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1. J Pediatr (1980) 1.10
Recurrent chromosomal defects are found in most patients with non-Hodgkin's-lymphoma. Cancer Genet Cytogenet (1984) 1.06
Alterations at the rel locus in human lymphoma. Oncogene (1991) 1.05
Human immunodeficiency virus gp120 binding C'C" ridge of CD4 domain 1 is also involved in interaction with class II major histocompatibility complex molecules. Proc Natl Acad Sci U S A (1992) 1.04
Trisomy for the proximal segment of the long arm of chromosome 13: a new entity? Am J Dis Child (1974) 1.02
Staining of satellite DNA in metaphase chromosomes. Nature (1971) 1.02
Chromosomal rearrangements, genes, and fragile sites in cancer: clinical and biologic implications. Important Adv Oncol (1986) 1.02
The G-banded prophase chromosomes of man. Humangenetik (1975) 1.01
Genes coding for histone proteins in man are located on the distal end of the long arm of chromosome 7. Science (1979) 0.99
Value of alkaline phosphatase, 5'-nucleotidase, gamma-glutamyltransferase, and glutamate dehydrogenase activity measurements (single and combined) in serum in diagnosis of metastasis to the liver. Clin Chem (1977) 0.99
A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10. J Pediatr (1974) 0.97
Phorbol ester-induced differentiation of a non-T, non-B leukemic cell line: model for human lymphoid progenitor cell development. J Immunol (1982) 0.97
Electrophoresis on cellulose acetate and chromatography on DEAE-sephadex A-50 compared in the estimation of creatine kinase isoenzymes. Clin Chem (1975) 0.97
Trisomy for the distal half of the short arm of chromosome 9. A variant of the trisomy 9p syndrome. Am J Dis Child (1976) 0.95
HLA-DQB1 allele typing by a new PCR-RFLP method: correlation with a PCR-SSO method. Tissue Antigens (1992) 0.95
Species and tissue specificity of very lysine-rich and serine-rich histones. Exp Cell Res (1969) 0.95
Molecular quantification of residual disease in chronic myelogenous leukemia after bone marrow transplantation. Blood (1992) 0.95
G-banding patterns of high-resolution human chromosomes 6--22, X, and Y. Hum Genet (1979) 0.94
Satellite DNA in calf heterochromatin. Exp Cell Res (1971) 0.93
Amplification and rearrangement of Hu-ets-1 in leukemia and lymphoma with involvement of 11q23. Science (1986) 0.93
Integration of avian sarcoma virus specific DNA in mammalian chromatin. Exp Cell Res (1975) 0.93
Identical MHC markers in non-Jewish Iranian and Ashkenazi Jewish patients with pemphigus vulgaris: possible common central Asian ancestral origin. Hum Immunol (1997) 0.92
Streptococcal nucleases. IV. Some properties and specificities of the ribonuclease action of the B and D enzymes. Biochemistry (1968) 0.92
Chromosomes and cancer: new nomenclature and future directions. Hum Pathol (1981) 0.91
High-resolution chromosomes as an independent prognostic indicator in adult acute nonlymphocytic leukemia. N Engl J Med (1984) 0.90
Deoxyribonucleic acid replication and mapping of the D-1 chromosome. A study of two patients with partial trisomy D-1. Am J Dis Child (1966) 0.90
Isolation of mammalian heterochromatin and euchromatin. Methods Cell Biol (1974) 0.89
Tumor necrosis factor constellation polymorphism and clozapine-induced agranulocytosis in two different ethnic groups. Blood (1997) 0.89
A common major histocompatibility complex class II allele HLA-DQB1* 0301 is present in clinical variants of pemphigoid. Proc Natl Acad Sci U S A (1996) 0.88
Major histocompatibility complex susceptibility genes for dermatitis herpetiformis compared with those for gluten-sensitive enteropathy. J Exp Med (1993) 0.87
Immunogenetics of atopic asthma: association of DRB1*1101 DQA1*0501 DQB1*0301 haplotype with Dermatophagoides spp.-sensitive asthma in a sample of the Venezuelan population. Clin Exp Allergy (1999) 0.87
Fragile sites and predisposition to leukemia and lymphoma. Cancer Genet Cytogenet (1984) 0.86
MLL tandem duplication and multiple splicing in adult acute myeloid leukemia with normal karyotype. Leukemia (1996) 0.85
Satellite DNA in mouse autosomal heterochromatin. Biochem Biophys Res Commun (1969) 0.85
G-banding and chromosome structure. Chromosoma (1973) 0.84
Improved blood RNA extraction microtechnique for RT-PCR. Biotechniques (1995) 0.83
On the kinetics of the Beckman enzymatic method for serum and urinary amylase. Clin Chem (1978) 0.83
The Philadelphia chromosome (Ph1) in adults presenting with acute leukaemia: a comparison of Ph1+ and Ph1-patients. Br J Haematol (1977) 0.83
High-resolution cytogenetics. Birth Defects Orig Artic Ser (1983) 0.81
DNA nucleotidylexotransferase of normal persons and leukemic patients. Clin Chem (1980) 0.81
Association study of polymorphisms in LRP1, tau and 5-HTT genes and Alzheimer's disease in a sample of Colombian patients. J Neural Transm (Vienna) (2005) 0.81
Cytological variations in the constitutive heterochromatin of Microtus agrestis. Chromosoma (1971) 0.81
Specific fine chromosomal defects in cancer: an overview. Hum Pathol (1981) 0.81
Pemphigus vulgaris autoantibody response is linked to HLA-DQB1*0503 in Pakistani patients. Hum Immunol (1997) 0.81
Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia. Cancer Genet Cytogenet (1984) 0.81
Prognostic significance of chromosomal abnormalities in acute leukaemias and myelodysplastic syndromes. Clin Haematol (1986) 0.81
Peripheral blood mononuclear cell adenosine deaminase activity in renal allograft recipients. J Surg Res (1978) 0.81
Adenosine deaminase activity in lymphocytes of normal persons, leukemic patients, and kidney-transplant recipients. Clin Chem (1977) 0.81
Serum guanase: a biochemical indicator of rejection in liver transplant recipients. Transplant Proc (1989) 0.80
Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantation. Birth Defects Orig Artic Ser (1986) 0.80
Clinical manifestations of mannosidosis--a longitudinal study. Am J Med (1976) 0.80
Comparative analysis of high-resolution chromosome techniques for leukemic bone marrows. Cancer Genet Cytogenet (1982) 0.80
Cloning and transcription factor-binding sites of the human c-rel proto-oncogene promoter. Gene (1996) 0.80
The Philadelphia chromosome in acute leukemia. Virchows Arch B Cell Pathol (1978) 0.80
Apolipoprotein E genotyping in a sample of Colombian patients with Alzheimer's disease. Neurosci Lett (2001) 0.79
Antenatal detection of partial C (6-12) trisomy. Lancet (1971) 0.79
Ocular cicatricial pemphigoid. A case report of monozygotic twins discordant for the disease. Arch Ophthalmol (1995) 0.79
Constitutive heterochromatin during early embryogenesis of Microtus agrestis. Exp Cell Res (1970) 0.78
A developmental study of constitutive heterochromatin in Microtus agrestis. Chromosoma (1971) 0.78
Rate of decay and distribution volume of MB isoenzyme of creatine kinase, intravenously injected into the baboon. Clin Chem (1976) 0.78
Mammalian X-chromosomes: change in patterns of DNA replication during embryogenesis. Science (1967) 0.78
Trisomy for the distal end of the short arm of chromosome 3: a syndrome. Am J Dis Child (1978) 0.78
Postsynthetic variants of creatine kinase MM. J Lab Clin Med (1981) 0.78