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Clinical Genetics|June 1, 1994
De novo isochromosome 18p in two patients: cytogenetic diagnosis and confirmation by chromosome paintingE Back, R Toder, I Voiculescu, et al.Clinical Genetics|June 1, 1994
Patient and parental attitudes toward genetic screening and its implications at an adult cystic fibrosis centreS P Conway, K Allenby, M N PondClinical Genetics|March 21, 2002
A PCR-based method for detecting known mutations in the human UDP galactose-4'-epimerase gene associated with epimerase-deficiency galactosemiaJ M Henderson, S M Huguenin, T M Cowan, et al.Clinical Genetics|March 21, 2002
Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4C R Hall, Y Wu, L G Shaffer, et al.Clinical Genetics|March 21, 2002
Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriagesS Yakut, S Berker-Karaüzüm, M Simşek, et al.Clinical Genetics|March 21, 2002
Fertility and pregnancy outcome in Danish women with Turner syndromeN H Birkebaek, D Crüger, J Hansen, et al.Clinical Genetics|March 21, 2002
A previously undescribed nonsense mutation of the HFE geneE Beutler, M J Griffin, T Gelbart, et al.Clinical Genetics|March 21, 2002
Distribution of HFE C282Y and H63D mutations in the Balearic Islands (NE Spain)P Guix, A Picornell, M Parera, et al.Clinical Genetics|March 21, 2002
Klinefelter syndrome is a common cause for mental retardation of unknown etiology among prepubertal malesM M Khalifa, J L StruthersClinical Genetics|March 21, 2002
Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patientsN Cine, A C Hatemi, N Erginel-UnaltunaPageof 718