Published in Cancer Genet Cytogenet on August 01, 1992
Bloom syndrome and maternal uniparental disomy for chromosome 15. Am J Hum Genet (1994) 0.88
Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus. EMBO J (1988) 3.82
Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA. Lancet (1993) 2.65
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. Am J Hum Genet (1996) 2.41
Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes. Am J Med Genet (1988) 2.00
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. Am J Hum Genet (1997) 1.99
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients. Am J Hum Genet (1995) 1.78
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. Am J Hum Genet (2000) 1.69
Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion. Am J Med Genet (1996) 1.67
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas. Prog Clin Biol Res (1989) 1.66
Bone marrow stromal cells regulate caspase 3 activity in leukemic cells during chemotherapy. Leuk Res (2001) 1.51
The syndromes of hydatidiform mole. I. Cytogenetic and morphologic correlations. Am J Obstet Gynecol (1978) 1.47
Three cases of tetrasomy 9p. Am J Med Genet (2002) 1.47
Retracted Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridization. Am J Med Genet (1996) 1.45
The syndromes of hydatidiform mole. II. Morphologic evolution of the complete and partial mole. Am J Obstet Gynecol (1978) 1.35
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers. Am J Hum Genet (1990) 1.25
The physical organization of the human immunoglobulin heavy chain gene complex. EMBO J (1990) 1.21
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype. Nat Genet (1994) 1.11
The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1. Clin Genet (1984) 1.09
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations. Am J Hum Genet (1994) 1.08
Application of chromosomal microarray in the evaluation of abnormal prenatal findings. Clin Genet (2012) 1.08
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn (1996) 1.01
Complete moles have paternal chromosomes but maternal mitochondrial DNA. Hum Genet (1982) 1.01
Two discrete regions of deletion at 7q in uterine leiomyomas. Genes Chromosomes Cancer (1997) 0.99
Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndrome. Am J Med Genet (1992) 0.98
Morphologic anomalies in triploid liveborn fetuses. Hum Pathol (1983) 0.98
X/Y translocations resulting from recombination between homologous sequences on Xp and Yq. Proc Natl Acad Sci U S A (1991) 0.97
A simplified six-item checklist for screening for fragile X syndrome in the pediatric population. J Pediatr (1996) 0.96
Chromosome mosaicism in hypomelanosis of Ito. Am J Med Genet (1990) 0.96
The clinicopathologic profile of the partial hydatidiform mole. Obstet Gynecol (1982) 0.96
Are the occasional aneuploid cells in peripheral blood cultures significant? Am J Med Genet (1984) 0.94
Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome. Am J Med Genet (1997) 0.93
Uterine leiomyomas: cytogenetic and histologic profile. Obstet Gynecol (1992) 0.93
Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92,XXXY karyotype. Hum Genet (1986) 0.93
Meiotic consequences of pericentric inversions of chromosome 13. Am J Med Genet (1981) 0.93
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas. Genes Chromosomes Cancer (1995) 0.93
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies. Hum Genet (2000) 0.92
Tissue culture of human renal epithelial cells using a defined serum-free growth formulation. Exp Nephrol (1999) 0.91
Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 cases. Cancer Genet Cytogenet (1991) 0.89
Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocation. Ophthalmic Paediatr Genet (1993) 0.87
The fragile X marker and autism in perspective. J Am Acad Child Adolesc Psychiatry (1989) 0.87
Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations. Placenta (2011) 0.87
The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome. Prenat Diagn (1997) 0.87
Deletion 7q22 in uterine leiomyoma. A cytogenetic review. Cancer Genet Cytogenet (1993) 0.86
Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue. Cancer Genet Cytogenet (1996) 0.86
Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors. Cancer Genet Cytogenet (1992) 0.86
Hydatidiform mole: cytogenetically unusual cases and their implications for the present classification. Am J Obstet Gynecol (1987) 0.86
Complete (classic) hydatidiform mole with 46,XY karyotype of paternal origin. Hum Genet (1979) 0.85
Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic events. Am J Med Genet A (2007) 0.85
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study. J Med Genet (2006) 0.84
Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistance. Cancer Genet Cytogenet (1998) 0.84
Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features. J Med Genet (1995) 0.84
Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors. Am J Med Genet (2002) 0.83
Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH). Am J Med Genet (1995) 0.83
Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome. Clin Genet (2000) 0.83
Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits. J Craniofac Genet Dev Biol (1996) 0.83
Myeloperoxidase-catalyzed redox-cycling of phenol promotes lipid peroxidation and thiol oxidation in HL-60 cells. Free Radic Biol Med (1999) 0.83
Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay. Genet Test (1999) 0.82
Involvement of 10q22 in leiomyoma. Cancer Genet Cytogenet (1993) 0.82
Case of Pallister-Killian syndrome with imperforate anus. Am J Med Genet (1988) 0.82
Mitogenic effect of basic fibroblast growth factor and estradiol on cultured human myometrial and leiomyoma cells. Am J Obstet Gynecol (1995) 0.82
Deletion of terminal portion of 6q: report of a case with unusual malformations. Am J Med Genet (1989) 0.82
Relaxation of imprinting in Prader-Willi syndrome. Hum Genet (1998) 0.82
Increased sister chromatid exchange frequency at Xq27 site in affected fragile X males. Am J Med Genet (1987) 0.81
Hydatidiform mole: parental chromosome aberrations in partial and complete moles. J Med Genet (1987) 0.81
Ring chromosome 1 in a newborn. Clin Dysmorphol (2000) 0.81
Genomic alterations in uterine leiomyosarcomas: potential markers for clinical diagnosis and prognosis. Genes Chromosomes Cancer (2001) 0.80
A molecular anatomical analysis of mosaic trisomy 16. Hum Genet (1996) 0.80
The cytogenetic, proliferative and viability effects of four bacteriophages on human lymphocytes. In Vitro (1978) 0.80
Chromosomal mapping of the human M6 genes. Genomics (1996) 0.79
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation. Am J Med Genet (1995) 0.79
Translocation (6;10)(p21;q22) in uterine leiomyomas. Cancer Genet Cytogenet (1995) 0.79
Patient with partial mole requiring chemotherapy. Lancet (1978) 0.78
A hypervariable region at the D19S11 locus. Hum Genet (1987) 0.78
Rearrangement of band 10q22 in leiomyoma and leiomyosarcoma of the uterus. Cancer Genet Cytogenet (1990) 0.78
Chromosome 7 biclonality in uterine leiomyoma. Cancer Genet Cytogenet (1993) 0.78
In vitro reversal of fragile-X expression by exogenous thymidine. Clin Genet (1984) 0.78
Cytogenetic analysis of a uterine lipoleiomyoma. Cancer Genet Cytogenet (1992) 0.78
Terminal 2q deletion--a recognizable syndrome. Clin Genet (1997) 0.78
Acrometageria: a spectrum of "premature aging" syndromes. Am J Med Genet (1992) 0.78
Deletion of chromosome 13 in leiomyomas of the uterus. Cancer Genet Cytogenet (1991) 0.78
Subgroups of uterine leiomyomas based on cytogenetic analysis. Hum Pathol (1991) 0.78
Strict clinicopathologic criteria in the diagnosis of partial hydatidiform mole: a plea renewed. Am J Obstet Gynecol (1985) 0.77
Chromosomal abnormalities in a psychiatric population. Am J Med Genet (1995) 0.77
Bacteriophages, vaccines, and people: an assessment of risk. Proc Soc Exp Biol Med (1978) 0.77
Spontaneous remission of infantile acute nonlymphocytic leukemia for 11 years in a child with normal karyotype. Cancer (1993) 0.77
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region. Am J Med Genet (1996) 0.77
Cytogenetic findings in a symplastic leiomyoma. Cancer Genet Cytogenet (1993) 0.77
Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosis. Gynecol Oncol (2003) 0.77
Cytogenetics and origins of pediatric germ cell tumors. Cancer Genet Cytogenet (1994) 0.77
Cytogenetic characterization of cat eye syndrome marker chromosome. Ann Genet (1994) 0.76
X chromosome imprinting in fragile X syndrome. Hum Genet (1990) 0.76
Complete and partial hydatidiform moles: cytogenetic and morphological aspects. Adv Exp Med Biol (1984) 0.76
Robertsonian translocations in Prader-Willi syndrome. Clin Genet (1991) 0.75
Rapid RFLP screening using DNA from complete hydatidiform moles. Nucleic Acids Res (1989) 0.75
Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma. Genomics (1998) 0.75
Sacral tumors in Schinzel-Giedion syndrome. Am J Med Genet (1998) 0.75
Fluorescent in situ hybridization for evaluation of Prader-Willi and Angelman syndromes. Am J Med Genet (1995) 0.75
Genetic analyses on a set of parasitic conjoined twins. Am J Med Genet (1992) 0.75
Assessment of X bends in patients with atypical X chromosome phenotypes. Ann Genet (1991) 0.75