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Human Genetics|June 1, 1996
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)M Erdel, S Schuffenhauer, B Buchholz, et al.Human Genetics|June 1, 1996
Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndromeS A Goodart, M G Butler, J OverhauserHuman Genetics|June 1, 1996
The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human spermM A Abruzzo, D K Griffin, E A Millie, et al.Human Genetics|June 1, 1996
Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7S Beck, F Badbanchi, M Otto, et al.Human Genetics|May 1, 1996
Assignment of the human ST2 gene to chromosome 2 at q11.2S Tominaga, J Inazawa, S TsujiHuman Genetics|May 1, 1996
Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmataT Hasegawa, T Ogata, Y Hasegawa, et al.Human Genetics|May 1, 1996
Fanconi anaemia in Italy: high prevalence of complementation group A in two geographic clustersA Savoia, A Zatterale, D Del Principe, et al.Human Genetics|May 1, 1996
Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragmentsI A Glass, M Passage, L Bernatowicz, et al.Human Genetics|May 1, 1996
Characterization of the human p57KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysisT Tokino, T Urano, T Furuhata, et al.Human Genetics|May 1, 1996
Distribution of mosaicism in human placentaeK G Henderson, T E Shaw, I J Barrett, et al.Pageof 959