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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 Human Genetics|November 1, 1992
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldismR A Spritz, S A Holmes, R Ramesar, 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.American Journal of Medical Genetics|October 1, 1990
Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagenI J Anderson, P Tsipouras, C Scher, et al.American Journal of Epidemiology|July 1, 1989
Recruiting survey respondents to mailed surveys: controlled trials of incentives and promptsV M Spry, M F Hovell, J G Sallis, 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.Journal of Medical Genetics|June 1, 1996
Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneityR S Ramesar, J Greenberg, R Martin, 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.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|March 5, 1988
Childhood deafness in ZimbabweD L Viljoen, G M Dent, A G Sibanda, 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.Pageof 23