Published in J Med Genet on September 01, 1972
Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome. J Med Genet (1981) 1.58
Comparison of adult height between patients with XX and XY gonadal dysgenesis: support for a Y specific growth gene(s). J Med Genet (1992) 1.13
Sexual and somatic determinants of the human Y chromosome: studies in a 46,XYp- phenotypic female. Am J Hum Genet (1979) 0.96
Deletion of the long arms of the Y chromosome with normal male development and intelligence. J Med Genet (1974) 0.92
Prenatal evaluation in a case of familial Y chromosome long arm deletion (Yq-). J Med Genet (1974) 0.83
Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardation. J Med Genet (1982) 0.80
FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY. J Med Genet (2000) 0.77
Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm. J Med Genet (1995) 0.75
Structural abnormalities of the Y chromosome in man. Nature (1966) 1.99
Deletion of Y chromosome in a family with muscular dystrophy and hypospadias. Br Med J (1962) 1.79
Definitive evidence for the short arm of the Y chromosome associating with the X chromosome during miosis in the human male. Nature (1970) 1.78
Chromosome studies on testicular cells from 50 subfertile men. Lancet (1966) 1.24
Males with an XYY sex chromosome complement. J Med Genet (1968) 1.22
Constancy of the length of human Y chromosome. Ann Genet (1969) 1.20
A familial Y-autosome translocation in man. Clin Genet (1971) 1.12
Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi). J Med Genet (1969) 1.03
X"Y"-XO MOSAICISM IN A PHENOTYPIC INTERSEX; REPORT OF A CASE. Am J Clin Pathol (1965) 1.00
The XYY chromosomal complement and nodulocystic acne. Ann Intern Med (1970) 0.87
Use of trypsin-modified human erythrocytes in rubella hemagglutination-inhibition testing. Appl Microbiol (1972) 3.81
HER-2/neu gene amplification characterized by fluorescence in situ hybridization: poor prognosis in node-negative breast carcinomas. J Clin Oncol (1997) 3.66
Cell culture of human colon adenomas and carcinomas. Cancer Res (1987) 2.68
Normal growth and differentiation in a spontaneously immortalized near-diploid human keratinocyte cell line, NIKS. J Invest Dermatol (2000) 2.08
Multidisciplinary approach to deep-seated lesions requiring radiologically-guided fine-needle aspiration. Diagn Cytopathol (1998) 2.04
Criteria for reporting fine needle aspiration on palpable and nonpalpable masses of the breast. Acta Cytol (1997) 1.96
The dup(3q) syndrome: report of eight cases and review of the literature. Am J Med Genet (1981) 1.52
Establishment and characterization of human colorectal cancer cell lines. Cancer Res (1984) 1.50
A juvenile polyposis tumor suppressor locus at 10q22 is deleted from nonepithelial cells in the lamina propria. Gastroenterology (1997) 1.46
Chromosomal instability in hereditary tyrosinemia type I. Pediatr Pathol (1990) 1.46
Aerosol transmission of rhinovirus colds. J Infect Dis (1987) 1.45
Establishment and characterization of an Epstein-Barr virus spontaneously transformed lymphocytic cell line derived from a hairy cell leukemia patient. Leukemia (1991) 1.41
Overcoming cellular senescence in human cancer pathogenesis. Genes Dev (1998) 1.36
Comparison of conventional Papanicolaou smears and a fluid-based, thin-layer system for cervical cancer screening. Obstet Gynecol (1997) 1.34
Methylation of the androgen receptor minimal promoter silences transcription in human prostate cancer. Cancer Res (2000) 1.30
Amplification in human breast cancer of a gene encoding a c-myc mRNA-binding protein. Cancer Res (2000) 1.25
Performance of liquid-based, thin-layer cervical cytology: correlation with reference diagnoses and human papillomavirus testing. Mod Pathol (1998) 1.22
Methylation of the androgen receptor promoter CpG island is associated with loss of androgen receptor expression in prostate cancer cells. Cancer Res (1998) 1.21
The trisomy 4p syndrome: case report and review. Am J Med Genet (1977) 1.20
A multicenter investigation with D-FISH BCR/ABL1 probes. Cancer Genet Cytogenet (2000) 1.16
The pallister mosaic syndrome. Birth Defects Orig Artic Ser (1977) 1.12
Improved dextran sulfate-calcium chloride method for the removal of nonspecific inhibitors with modifications for nonspecific agglutinin removal in the rubella hemagglutination inhibition test. Appl Microbiol (1972) 1.12
Use of FISH to detect chromosomal translocations and deletions. Analysis of chromosome rearrangement in synovial sarcoma cells from paraffin-embedded specimens. Am J Pathol (1993) 1.07
A bacteriologic study of Madison area beaches. Wis Med J (1973) 1.03
Extensive amplification of bcr/abl fusion genes clustered on three marker chromosomes in human leukemic cell line K-562. Leukemia (1995) 0.99
Synovial sarcoma of the upper digestive tract: a report of two cases with demonstration of the X;18 translocation by fluorescence in situ hybridization. Mod Pathol (2000) 0.97
Compatibility of trypsin-modified human erythrocytes in the rubella hemagglutination-inhibition test employing three serum treatment procedures. Appl Microbiol (1974) 0.97
A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings. J Pediatr (1965) 0.95
Thyroid status and thermogenesis in rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin. Toxicol Appl Pharmacol (1986) 0.94
Neoplastic transformation of SV40-immortalized human urinary tract epithelial cells by in vitro exposure to 3-methylcholanthrene. Carcinogenesis (1988) 0.94
Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocation. Clin Genet (1982) 0.94
A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19). Clin Genet (1974) 0.93
Interruption of transmission of rhinovirus colds among human volunteers using virucidal paper handkerchiefs. J Infect Dis (1986) 0.93
Study of mycoplasma in university students with non-gonococcal urethritis. Health Lab Sci (1971) 0.92
Screening parameters for ThinPrep and conventional gynecologic cytology via automated monitoring. Acta Cytol (2000) 0.90
Letter: Trisomy-20 syndrome in man. Lancet (1976) 0.89
Banding of human chromosomes with caesium chloride. Lancet (1973) 0.88
Use of fluorescence in situ hybridization for retrospective detection of aneuploidy in multiple myeloma. Genes Chromosomes Cancer (1993) 0.88
Serum cholesterol levels of Mexican and Wisconsin school children. Am J Epidemiol (1972) 0.88
Attenuated influenza A vaccine (Alice) in an adult population: vaccine-related illness, serum and nasal antibody production, and intrafamily transmission. J Clin Microbiol (1975) 0.87
Short- and long-term estrogen deprivation of T47D human breast cancer cells in culture. Eur J Cancer Clin Oncol (1989) 0.87
'Expanded' Prader-Willi syndrome in a boy with an unusual 15q chromosome deletion. Am J Dis Child (1983) 0.86
Comparison of chromosome aberrations in leiomyoma and leiomyosarcoma using FISH on archival tissues. Cancer Genet Cytogenet (1994) 0.86
Detection of aneuploidy and possible deletion in paraffin-embedded rhabdomyosarcoma cells with FISH. Cancer Genet Cytogenet (1993) 0.86
Absorbed heterophile and ox-cell hemolysin test in serodiagnosis of infectious mononucleosis. Health Lab Sci (1975) 0.85
Rare clonal karyotypic variants in primary cultures of human breast carcinoma cells. Cancer Res (1989) 0.85
Serologic study of specimens with borderline FTA-ABS test reactivity. Health Lab Sci (1977) 0.85
Toward quality assurance for metaphase FISH: a multicenter experience. Am J Med Genet (1996) 0.84
Follow-up on a human X-autosome translocation first studied in 1963 and 1964. Birth Defects Orig Artic Ser (1978) 0.83
Prevalence of antibodies to Epstein-Barr virus, cytomegalovirus and Toxoplasma in a Mexican highland community. Am J Epidemiol (1973) 0.83
Establishment and characterization of a SV40 T-antigen immortalized human bronchial epithelial cell line. In Vitro Cell Dev Biol (1992) 0.82
Giemsa banding specificity. Nat New Biol (1973) 0.82
Evaluation of cholesterol determinations among clinical laboratories in Wisconsin. Public Health Rep (1967) 0.82
Synergistic effect of TPA and T-cell mitogens in nonmammalian vertebrates. In Vitro (1984) 0.82
Hypophagia-induced weight loss in mice, rats, and guinea pigs treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin. Fundam Appl Toxicol (1985) 0.81
Near disappearance of rhinovirus along a fomite transmission chain. J Infect Dis (1988) 0.81
Standards of adequacy of cytologic examination of the female genital tract. Am J Clin Pathol (1974) 0.80
Chromosome banding in G 2 with tetracycline. Lancet (1973) 0.80
Relationship of the wasting syndrome to lethality in rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin. Toxicol Appl Pharmacol (1986) 0.80
Emergence of acute non-lymphocytic leukemia in breast cancer patients. Am J Med Sci (1982) 0.79
Cytogenetic studies of herbicide interactions in vitro and in vivo using atrazine and linuron. Arch Environ Contam Toxicol (1992) 0.79
Karyotype evolution of cells with the Philadelphia chromosome. Acta Cytol (1970) 0.79
Marker chromosome stability associated with neoplastic transformation of human uroepithelial cells. Cancer Genet Cytogenet (1988) 0.79
Adenocarcinoma of the prostate in a 41-year-old man with XXY karyotype and chronic lymphocytic leukemia: report of a case. J Urol (1991) 0.79
Losses of 3p, 11p, and 13q in EJ/ras-transformable simian virus 40-immortalized human uroepithelial cells. Genes Chromosomes Cancer (1992) 0.79
Microanalysis of chromosomes with x-ray energy dispersion. Lancet (1973) 0.79
Mechanism of trypsin chromosome banding. Lancet (1973) 0.78
Nonrandom chromosome losses in stepwise neoplastic transformation in vitro of human uroepithelial cells. Cancer Res (1991) 0.78
A state-wide proficiency testing program in cytology. Acta Cytol (1972) 0.78
Use of nonbreakpoint DNA probes to detect the t(X;18) in interphase cells from synovial sarcoma: implications for detection of diagnostic tumor translocations. Am J Pathol (1998) 0.78
Toward quality assurance for metaphase FISH: a multi-center experience. Am J Med Genet (1996) 0.78
Genetic mechanisms in cancer predisposition: report of a cancer family. Cancer (1979) 0.78
Chromosomal protein and C-banding. Lancet (1973) 0.78
Behavioral retardation in a macaque with autosomal trisomy and aging mother. Am J Ment Retard (1996) 0.77
Serologic profile of children in a Mexican highland community: prevalence of complement-fixing antibodies to Mycoplasma pneumoniae, respiratory syncytial virus and parainfluenza viruses. Am J Epidemiol (1975) 0.77
Cell volume distribution pattern analysis: a means of uterine cancer detection. Am J Clin Pathol (1970) 0.77
Effect of interferon alpha, interferon beta, and interferon gamma on the in vitro growth of human renal adenocarcinoma cells. Invest New Drugs (1987) 0.77
Comparison of prometaphase chromosome techniques with emphasis on the role of colcemid. In Vitro (1984) 0.77
Olfactory neuroblastoma (esthesioneuroblastoma): appearance on fine-needle aspiration: report of a case. Diagn Cytopathol (1997) 0.76
EJ/ras neoplastic transformation of simian virus 40-immortalized human uroepithelial cells: a rare event. Cancer Res (1990) 0.76
FISH detection of HER-2/neu oncogene amplification in early onset breast cancer. Breast Cancer Res Treat (1996) 0.76
Effects of perfluorodecanoic acid on thyroid status in rats. Toxicol Appl Pharmacol (1987) 0.76
A perspective on modern quality control methods. Acta Cytol (1996) 0.75
Friedan and estrogen: 'most unfortunate that she is so misinformed'. Geriatrics (1994) 0.75
Assessing aneuploidy in normal tissues with FISH: pitfalls and insights. Cancer Genet Cytogenet (1994) 0.75
DNA polymerase alpha defect in the N syndrome. Am J Med Genet (1990) 0.75
Dye-nucleoprotein interactions in Giemsa banding. J Cell Biol (1974) 0.75
Fragile X frequency. Am J Med Genet (1990) 0.75
Newborn infant with del(9)(pter----q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary ears. Am J Med Genet Suppl (1987) 0.75
Mechanisms of chromatid breakage in human lymphocyte cultures. Acta Cytol (1977) 0.75
Scanning electron microscopy after cytologic examination of urinary cells: lack of diagnostic advantage using combined microscopy. Acta Cytol (1982) 0.75
Wisconsin's laboratory evaluation and certification program. Health Lab Sci (1977) 0.75