Genetic analysis of repeated, biparental, diploid, hydatidiform moles.
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L. Bolund | L. Sunde | J. Hertz | M. Jensen | S. Pedersen | L. Vejerslev
[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 .