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Clinical Genetics|May 1, 1989
Radial ray defects and associated anomaliesH Cox, D Viljoen, G Versfeld, et al.Clinical Genetics|January 1, 1987
Heterozygous manifestations of Langer mesomelic dysplasiaJ Goldblatt, C Wallis, D Viljoen, et al.American Journal of Medical Genetics|April 1, 1987
Familial rhizomelic dysplasia: phenotypic variation or heterogeneity?D Viljoen, J Goldblatt, C Wallis, et al.American Journal of Medical Genetics|December 31, 1997
Mseleni and Handigodu familial osteoarthropathies: syndromic identity?S S Agarwal, S R Phadke, V Fredlund, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 26, 1985
Ectrodactyly in central AfricaD Viljoen, H M Farrell, J J Brossy, et al.American Journal of Medical Genetics|June 1, 1989
Two rare developmental defects of the lower limbs with confirmation of the Lewin and Opitz hypothesis on the fibular and tibial developmental fieldsL Pavone, D Viljoen, S Ardito, et al.Journal of Medical Genetics|June 1, 1993
Osteogenesis imperfecta type III: mutations in the type I collagen structural genes, COL1A1 and COL1A2, are not necessarily responsibleG A Wallis, B Sykes, P H Byers, et al.Annals of the New York Academy of Sciences|January 1, 1991
Hearing impairment and pigmentary disturbanceP Beighton, R Ramesar, I Winship, et al.Journal of Medical Genetics|December 10, 1997
Familial streptomycin ototoxicity in a South African family: a mitochondrial disorderJ C Gardner, R Goliath, D Viljoen, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 1, 1996
Mseleni joint disease--a molecular genetic approach to defining the aetiologyR Ballo, D Viljoen, M Machado, et al.Pageof 26