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Journal of Medical Genetics|August 1, 1980
45,X/46,XY/47,XY, +21 mosaicism in a hypogonadal phenotypic maleM Sparagana, P W Wong, T R Dorsch, et al.Journal of Medical Genetics|February 1, 1984
The origin of ovarian teratomasJ M Parrington, L F West, S PoveyJournal of Medical Genetics|April 1, 1978
Shifting genetic patterns in anencephaly and spina bifidaD T Janerich, J PiperJournal of Medical Genetics|April 1, 1978
Genetic counseling of consanguineous families. Use of Smith's method to calculate recurrence risks in multifactorial inheritance in consanguineous matingsC BonaitiJournal of Medical Genetics|April 1, 1978
Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicismE W Naylor, W H Murphey, E I Domoszlai, et al.Journal of Medical Genetics|October 1, 1981
5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardationN Tommerup, H Poulsen, K Brøndum-NielsenJournal of Medical Genetics|October 1, 1981
Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatallyA M Migliorini, R Coco, T C De Negrotti, et al.Journal of Medical Genetics|October 28, 2009
Clinical and molecular characterisation of Bardet-Biedl syndrome in consanguineous populations: the power of homozygosity mappingL Abu Safieh, M A Aldahmesh, H Shamseldin, et al.Pageof 649