Published in Cancer Genet Cytogenet on April 01, 1987
Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis. Br J Cancer (1992) 3.10
Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome. Am J Hum Genet (1995) 1.22
Gonadoblastoma, testicular and prostate cancers, and the TSPY gene. Am J Hum Genet (1999) 1.08
Constitutional aneuploidy and cancer predisposition. Hum Mol Genet (2009) 1.05
Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK. Arch Dis Child (1997) 1.00
The Y-encoded TSPY protein: a significant marker potentially plays a role in the pathogenesis of testicular germ cell tumors. Hum Pathol (2007) 0.97
Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies. J Med Genet (1992) 0.94
Occurrence of cancer in women with Turner syndrome. Br J Cancer (1996) 0.93
Testicular microlithiasis as a familial risk factor for testicular germ cell tumour. Br J Cancer (2007) 0.90
Surgical management of ambiguous genitalia. Arch Dis Child (2003) 0.86
A physical analysis of the Y chromosome shows no additional deletions, other than Gr/Gr, associated with testicular germ cell tumour. Br J Cancer (2007) 0.85
Inguinal lymph node metastases from a testicular seminoma: a case report and a review of the literature. J Med Case Rep (2010) 0.85
State of the art review in gonadal dysgenesis: challenges in diagnosis and management. Int J Pediatr Endocrinol (2014) 0.83
An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes. J Med Genet (1991) 0.82
Tumors of bilateral streak gonads in patients with disorders of sex development containing y chromosome material. Clin Pediatr Endocrinol (2014) 0.82
Gonadoblastoma: evidence for a stepwise progression to dysgerminoma in a dysgenetic ovary. Virchows Arch (2005) 0.79
Human Y-chromosome variation and male dysfunction. J Mol Genet Med (2005) 0.79
An improved, non-isotopic method of screening cells from patients with abnormalities of sexual differentiation for Y chromosomal DNA content. J Med Genet (1993) 0.78
A rare case of mixed gonadal dysgenesis with mosaicism 45, X/46, X, +mar. Int J Surg Case Rep (2014) 0.78
Detection of Y mosaicism in patients with Turner's syndrome. J Med Genet (1995) 0.77
Dysgerminoma in a female with turner syndrome and Y chromosome material: A case-based review of literature. Indian J Endocrinol Metab (2012) 0.76
Management of a 3-year-old child with ambiguous genitalia. Urol Ann (2015) 0.75
The role of sex chromosomes in mammalian germ cell differentiation: can the germ cells carrying X and Y chromosomes differentiate into fertile oocytes? Asian J Androl (2015) 0.75
Hidden Y Chromosome Mosaicism in 48 Egyptian Patients with Turner's Syndrome. Genet Res Int (2013) 0.75
A male phenotype (XY) hermaphrodite treated for seminoma, fathered a healthy child by IVF-ICSI technique. J Assist Reprod Genet (2008) 0.75
Mixed Germ Cell Tumour in a Case of Pure Gonadal Dysgenesis (Swyer Syndrome) - A Case Report. Cureus (2016) 0.75
Evaluation and treatment for ovotesticular disorder of sex development (OT-DSD) - experience based on a Chinese series. BMC Urol (2017) 0.75
Androgen insensitivity syndrome. Arch Dis Child (1993) 0.75
Embryology and adult urology - Not always mutually exclusive: A case report on true hermaphroditism at an adult urology clinic. Can Urol Assoc J (2014) 0.75
Association of immunohistochemical markers with premalignancy in Gonadal Dysgenesis. Int J Pediatr Endocrinol (2015) 0.75
Bilateral Sertoli Cell Tumors in a Patient with Androgen Insensitivity Syndrome. Case Rep Obstet Gynecol (2017) 0.75
Malignancy in disorders of sex development. Transl Androl Urol (2016) 0.75
Molecular biology of Turner's syndrome. Arch Dis Child (1995) 0.75
Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study). Ther Clin Risk Manag (2017) 0.75
The absence of a relation between the periconceptional use of vitamins and neural-tube defects. National Institute of Child Health and Human Development Neural Tube Defects Study Group. N Engl J Med (1989) 3.82
The overlap syndrome of asthma and COPD: what are its features and how important is it? Thorax (2009) 3.30
Heterogeneity of airway inflammation in persistent asthma : evidence of neutrophilic inflammation and increased sputum interleukin-8. Chest (2001) 3.19
Sex ratio associated with timing of insemination and length of the follicular phase in planned and unplanned pregnancies during use of natural family planning. Hum Reprod (1998) 2.67
Are obese women at higher risk for producing malformed offspring? Am J Obstet Gynecol (1994) 2.31
Moderate caffeine use and the risk of spontaneous abortion and intrauterine growth retardation. JAMA (1993) 2.20
Down syndrome is not increased in offspring of natural family planning users (case control analysis) Am J Med Genet (1995) 2.13
Gamma delta T cells in human decidua. Am J Obstet Gynecol (1993) 2.06
Neutrophil degranulation and cell lysis is associated with clinical severity in virus-induced asthma. Eur Respir J (2002) 1.92
Soluble RAGE is deficient in neutrophilic asthma and COPD. Eur Respir J (2011) 1.76
Genetically determined sex-reversal in 46,XY humans. Science (1978) 1.76
Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study. Prenat Diagn (2002) 1.74
Heritable aspects of endometriosis. I. Genetic studies. Am J Obstet Gynecol (1980) 1.60
Different inflammatory phenotypes in adults and children with acute asthma. Eur Respir J (2011) 1.50
Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis. N Engl J Med (1988) 1.50
Risk of neural tube defects in relation to maternal fertility and fertility drug use. Lancet (1990) 1.49
Shared HLA antigens and reproductive performance among Hutterites. Am J Hum Genet (1983) 1.47
A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group. N Engl J Med (1992) 1.43
Metabolic control and progression of retinopathy. The Diabetes in Early Pregnancy Study. National Institute of Child Health and Human Development Diabetes in Early Pregnancy Study. Diabetes Care (1995) 1.42
Chorionic villus sampling for first-trimester prenatal diagnosis: Northwestern University program. Am J Obstet Gynecol (1985) 1.42
Pregnancy and the timing of intercourse. N Engl J Med (1995) 1.41
Risk evaluation of CVS. Prenat Diagn (1993) 1.40
Low maternal serum alpha-fetoprotein and perinatal outcome. Am J Obstet Gynecol (1987) 1.39
Risk of recurrent spontaneous abortion for pregnancies discovered in the fifth week of gestation. Lancet (1994) 1.37
Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn (1992) 1.35
Maternal serum screening for fetal Down syndrome in women less than 35 years of age using alpha-fetoprotein, hCG, and unconjugated estriol: a prospective 2-year study. Obstet Gynecol (1992) 1.34
Heritability and molecular genetic studies of endometriosis. Hum Reprod Update (2000) 1.30
Prenatal diagnosis by use of fetal cells isolated from maternal blood. Am J Obstet Gynecol (1995) 1.29
Resorbed co-twin as an explanation for discrepant chorionic villus results: non-mosaic 47,XX,+16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal blood. Prenat Diagn (1989) 1.27
A previously unrecognized X-linked syndrome of dysmorphia. Birth Defects Orig Artic Ser (1975) 1.22
Incidence of spontaneous abortion among normal women and insulin-dependent diabetic women whose pregnancies were identified within 21 days of conception. N Engl J Med (1988) 1.22
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients. Am J Med Genet (2001) 1.16
Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis. J Med Genet (1996) 1.13
Frequency of diabetes mellitus in mothers of probands with gestational diabetes: possible maternal influence on the predisposition to gestational diabetes. Am J Obstet Gynecol (1985) 1.10
Patient or physician preferences for decision analysis: the prenatal genetic testing decision. Med Decis Making (1999) 1.08
Sister chromatid exchanges after exposure to ultrasound and mitomycin C. Am J Obstet Gynecol (1984) 1.07
Gender verification of female athletes. Genet Med (2001) 1.07
Adverse outcomes of planned and unplanned pregnancies among users of natural family planning: a prospective study. Am J Public Health (1997) 1.06
Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data. Birth Defects Orig Artic Ser (1971) 1.05
Adverse effects of human leukocyte antigen-DR sharing on fertility: a cohort study in a human isolate. Fertil Steril (1985) 1.04
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. Am J Hum Genet (1993) 1.01
Late first-trimester invasive prenatal diagnosis: results of an international randomized trial. Obstet Gynecol (2004) 1.01
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn (1996) 1.01
Heritage aspects of endometriosis. II. Clinical characteristics of familial endometriosis. Am J Obstet Gynecol (1980) 1.01
Cancers of the breast and female genital system: search for recessive genetic factors through analysis of human isolate. Am J Obstet Gynecol (1981) 1.00
HLA-G1 protein expression is not essential for fetal survival. Placenta (1998) 1.00
Physiological reduction in fasting plasma glucose concentration in the first trimester of normal pregnancy: the diabetes in early pregnancy study. Metabolism (1998) 1.00
Testicular feminisation and inguinal hernia. Lancet (1973) 0.98
The relationship of neoplasia to disorders of abnormal sexual differentiation. Birth Defects Orig Artic Ser (1976) 0.98
Prenatal diagnosis of harlequin ichthyosis. Clin Genet (1980) 0.96
Current status of preimplantation diagnosis. J Assist Reprod Genet (1997) 0.96
Re: Update on MSAFP Policy Statement from the ASHG. Am J Hum Genet (1990) 0.96
Pseudovaginal perineoscrotal hypospadias. Clin Genet (1972) 0.96
Declining insulin requirement in the late first trimester of diabetic pregnancy. Diabetes Care (2001) 0.95
Full blood count parameters for the detection of asthma inflammatory phenotypes. Clin Exp Allergy (2014) 0.95
Parental decision following prenatal diagnosis of fetal chromosome abnormality. Am J Med Genet (1988) 0.94
XY gonadal dysgenesis: genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis. Hum Genet (1981) 0.94
A child with facial and skeletal dysmorphia reminiscent of Schwartz syndrome. Birth Defects Orig Artic Ser (1975) 0.93
Induction of gamma-glutamyl transpeptidase mRNA by aflatoxin B1 and ethoxyquin in rat liver. Carcinogenesis (1987) 0.93
Induced sputum IL-8 gene expression, neutrophil influx and MMP-9 in allergic bronchopulmonary aspergillosis. Eur Respir J (2003) 0.92
Rare event selection of fetal nucleated erythrocytes in maternal blood by flow cytometry. Cytometry (1996) 0.92
Prenatal effects of maternal-fetal HLA compatibility. Am J Reprod Immunol Microbiol (1987) 0.92
Relationship between induced sputum eosinophils and the clinical pattern of childhood asthma. Thorax (2003) 0.92
Safety of sputum induction with isotonic saline in adults with acute severe asthma. Clin Exp Allergy (2001) 0.92
Preferences of pregnant women for amniocentesis or chorionic villus sampling for prenatal testing: comparison of patients' choices and those of a decision-analytic model. J Clin Epidemiol (1994) 0.92
Characterization of innate immune signalling receptors in virus-induced acute asthma. Clin Exp Allergy (2010) 0.91
First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood. Lancet (1992) 0.91
Gender testing in the Olympics. JAMA (1986) 0.90
Isolated fetal choroid plexus cysts and trisomy 18: a review and meta-analysis. Am J Obstet Gynecol (1995) 0.90
A prospective trial of prenatal screening for Down syndrome by means of maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated estriol. Am J Obstet Gynecol (1993) 0.90
Timing of conception and the risk of spontaneous abortion among pregnancies occurring during the use of natural family planning. Am J Obstet Gynecol (1995) 0.90
Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam. Ann Genet (1973) 0.89
Differential gene expression and cytokine production from neutrophils in asthma phenotypes. Eur Respir J (2009) 0.89
Amniocentesis or chorionic villus sampling for prenatal genetic testing: a decision analysis. J Clin Epidemiol (1991) 0.89
Hereditary aspects of ovarian and testicular neoplasia. Birth Defects Orig Artic Ser (1976) 0.88
Gonadal dysgenesis as an autosomal recessive condition. Am J Obstet Gynecol (1969) 0.88
Unintended pregnancies in women delivering at 18 South American hospitals. NFP-ECLAMC Group. Latin American Collaborative Study of Congenital Malformations. Hum Reprod (1998) 0.88
More than we ever wanted to know about sex--should we be afraid to ask? N Engl J Med (1979) 0.88
Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation. Birth Defects Orig Artic Ser (1975) 0.88
Abnormal sexual differentiation in humans. Annu Rev Genet (1982) 0.87
Noninvasive determination of fetal RhD status using fetal DNA in maternal serum and PCR. J Soc Gynecol Investig (1999) 0.87
Fetal cells in the maternal circulation: isolation by multiparameter flow cytometry and confirmation by polymerase chain reaction. Hum Reprod (1991) 0.87
Genetic amniocentesis in twin gestations. Am J Obstet Gynecol (1980) 0.87
Parental chromosomal rearrangements associated with repetitive spontaneous abortions. Fertil Steril (1981) 0.86
Chromosome analysis of ectopic human conceptuses. Am J Obstet Gynecol (1981) 0.85
Airway eosinophilia is associated with wheeze but is uncommon in children with persistent cough and frequent chest colds. Am J Respir Crit Care Med (2001) 0.85
Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic-karyotypic correlations. Birth Defects Orig Artic Ser (1975) 0.85
A null mutation in HLA-G is not associated with preeclampsia or intrauterine growth retardation. J Reprod Immunol (2000) 0.84
Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies. Fertil Steril (1983) 0.84
Developmental regulation of the catalytic subunit of the apolipoprotein B mRNA editing enzyme (APOBEC-1) in human small intestine. J Lipid Res (1995) 0.84
Fetal surgery for myelomeningocele: promise, progress, and problems. JAMA (1999) 0.84
Increased heterogeneity of chromosome 17 aneuploidy in endometriosis. Am J Obstet Gynecol (1999) 0.83
Relationship between Y-chromosome length and first-trimester spontaneous abortions. Am J Obstet Gynecol (1983) 0.83
Current progress in preimplantation genetic diagnosis. J Assist Reprod Genet (1993) 0.83
Endometrial adenocarcinoma: genetic analysis suggesting heritable site-specific uterine cancer. Gynecol Oncol (1992) 0.83
Cellular response in rabbit eyes after human fetal RPE cell transplantation. Graefes Arch Clin Exp Ophthalmol (1999) 0.83
Genes, chromosomes, and reproductive failure. Fertil Steril (1980) 0.83