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Clinical Genetics|December 1, 1993
Insertion/deletion (I/D) polymorphism at the locus for angiotensin I-converting enzyme and parental history of myocardial infarctionM Bøhn, K E Berge, A Bakken, et al.Clinical Genetics|December 1, 1993
Immunofluorescence imaging diagnosis of Fabry heterozygotes using confocal laser scanning microscopyK Itoh, M Kotani, T Tai, et al.Clinical Genetics|June 1, 1984
Renal agenesis as a diagnostic feature of the cryptophthalmos-syndactyly syndromeI W Lurie, E D CherstvoyClinical Genetics|January 1, 1995
Increased frequency of the rare PstI allele (P2) in a population of CAD patients in northern GreeceN A Vavatsi, S A Kouidou, P N Geleris, et al.Clinical Genetics|January 1, 1995
Familial microcephaly with severe neurological deficits: a description of five affected siblingsV Gross-Tsur, A Joseph, G Blinder, et al.Clinical Genetics|January 1, 1995
Dicentric chromosome Y associated with Leydig cell agenesis and sex reversalM Genuardi, B Bardoni, G Floridia, et al.Clinical Genetics|January 1, 1995
Factors influencing whether or not couples seek genetic counselling: an explorative study in a paediatric surgical unitI Hobus, P G Frets, H J Duivenvoorden, et al.Clinical Genetics|January 1, 1995
Antley-Bixler syndrome and esophageal atresia in a patient with trisomy 21E Feigin, R Udassin, D Seror, et al.Clinical Genetics|November 1, 1984
ATPase activity of erythrocyte membrane in patients with trisomy 21 (Down's syndrome)Q M Xue, D G Shen, W DongPageof 718