Genetic analysis of repeated, biparental, diploid, hydatidiform moles.

[1]  L. Sunde Genetic analyses of hydatidiform moles with conceptual and practical implications , 1994 .

[2]  I. Christensen,et al.  Hydatidiform Mole and Fetus With Normal Karyotype: Support of a Separate Entity , 1991, Obstetrics and gynecology.

[3]  K. Kidd,et al.  Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14) , 1990 .

[4]  Y. Nakamura,et al.  Molecular evidence that homologous recombination occurs in proliferating human somatic cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[5]  M. Monk,et al.  Variation in epigenetic inheritance. , 1990, Trends in genetics : TIG.

[6]  M. Lyon,et al.  Chromosome maps of man and mouse. IV , 1989, Annals of human genetics.

[7]  H. Saal,et al.  Molar pregnancy coexisting with a normal fetus: a case report. , 1989, Gynecologic oncology.

[8]  L. Bolund,et al.  Genetically different cell subpopulations in hydatidiform moles. A study of three cases by RFLP, flow cytometric, cytogenetic, HLA, and morphologic analyses. , 1989, Cancer genetics and cytogenetics.

[9]  S. Latt,et al.  Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. , 1989, American journal of medical genetics.

[10]  Côté Gb Wilms' tumour and related syndromes. A unifying theory. , 1989 .

[11]  S. Godfrey,et al.  Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans? , 1989, American journal of human genetics.

[12]  W. Reik Genomic imprinting and genetic disorders in man. , 1989, Trends in genetics : TIG.

[13]  W. Reik Genomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea. , 1988, Journal of medical genetics.

[14]  J. Hobbins,et al.  SONOGRAPHIC DIAGNOSIS OF A PREGNANCY WITH A DIFFUSE HYDATIDIFORM MOLE AND COEXISTENT 46,XX FETUS: A CASE REPORT , 1988, Obstetrics and gynecology.

[15]  P M Conneally,et al.  Anticipation in Huntington's disease is inherited through the male line but may originate in the female. , 1988, Journal of medical genetics.

[16]  D. Ledbetter,et al.  Uniparental disomy as a mechanism for human genetic disease. , 1988, American journal of human genetics.

[17]  A. Jeffreys,et al.  Characterization of a panel of highly variable minisatellites cloned from human DNA , 1987, Annals of human genetics.

[18]  D. Simon,et al.  Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation , 1987, Nature.

[19]  Driscoll Sg Problems and pitfalls in the histopathologic diagnosis of gestational trophoblastic lesions. , 1987 .

[20]  P. Leder,et al.  Parental legacy determines methylation and expression of an autosomal transgene: A molecular mechanism for parental imprinting , 1987, Cell.

[21]  N. Tommerup,et al.  DNA-aneuploidy in 46,XX hydatidiform moles. , 1987, Cancer genetics and cytogenetics.

[22]  C. Sapienza,et al.  Degree of methylation of transgenes is dependent on gamete of origin , 1987, Nature.

[23]  M. Surani,et al.  Genomic imprinting determines methylation of parental alleles in transgenic mice , 1987, Nature.

[24]  U. Surti,et al.  Hydatidiform mole: cytogenetically unusual cases and their implications for the present classification. , 1987, American journal of obstetrics and gynecology.

[25]  R. Fisher,et al.  Genetic studies in hydatidiform mole with clinical correlations. , 1987, Placenta.

[26]  B. Cattanach Parental origin effects in mice. , 1986, Journal of embryology and experimental morphology.

[27]  M. Surani,et al.  Nuclear transplantation in the mouse: Heritable differences between parental genomes after activation of the embryonic genome , 1986, Cell.

[28]  L. Peters,et al.  Flow cytometric analysis of head and neck carcinoma DNA index and S-fraction from paraffin-embedded sections: comparison with malignancy grading. , 1985, Cytometry.

[29]  U. Surti,et al.  Strict clinicopathologic criteria in the diagnosis of partial hydatidiform mole: a plea renewed. , 1985, American journal of obstetrics and gynecology.

[30]  N. Teng,et al.  Partial hydatidiform mole with diploid karyotype: report of three cases. , 1984, American journal of obstetrics and gynecology.

[31]  M. Lyon,et al.  Chromosome maps of man and mouse , 1981, Clinical genetics.

[32]  Dodson Mg New concepts and questions in gestational trophoblastic disease. , 1983 .

[33]  U. Surti,et al.  The syndromes of hydatidiform mole. II. Morphologic evolution of the complete and partial mole. , 1978, American journal of obstetrics and gynecology.

[34]  U. Surti,et al.  The syndromes of hydatidiform mole. I. Cytogenetic and morphologic correlations. , 1978, American journal of obstetrics and gynecology.

[35]  Nielsen Nj Hydatiform mole with a living infant , 1972 .

[36]  J. Langman Medical Embryology: Human Development-Nor mal and Abnormal , 1964 .