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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.British Medical Journal|May 12, 1979
Prospective study of genetic counsellingA E Emery, J A Raeburn, R Skinner, 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.American Journal of Medical Genetics|September 1, 1982
AtelosteogenesisP Maroteaux, J Spranger, V Stanescu, et al.The EMBO Journal|July 1, 1985
Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfectaA F Grobler-Rabie, G Wallis, D K Brebner, et al.American Journal of Obstetrics and Gynecology|May 15, 1982
Prenatal diagnosis of Duchenne muscular dystrophy: failure of amniotic fluid and maternal serum N tau-methylhistidine analyses to detect affected fetusesS J Wassner, J B Li, R L Ladda, et al.Pageof 28