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Journal of the Neurological Sciences|December 1, 1976
International collaborative study of the spinal muscular atrophies. Part 2. Analysis of genetic dataA E Emery, A M Davie, S Holloway, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|November 24, 1984
Pseudoxanthoma elasticum in South Africa--genetic and clinical implicationsD L Viljoen, P Beighton, T Mabin, et al.
American Journal of Human Genetics|June 7, 2000
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27P Ianakiev, M W Kilpatrick, I Toudjarska, et al.
The British Journal of Radiology|June 1, 1979
The radiological manifestations of metaphyseal dysplasia (Pyle disease)N G Heselson, M S Raad, H Hamersma, et al.
Lancet (London, England)|March 4, 1978
Aryl-hydrocarbon-hydroxylase inducibility in patients with cancerA E Emery, R Anand, N Danford, et al.
Palliative Medicine|January 1, 1994
Communication with parents of children with cancerO B Eden, I Black, G A MacKinlay, et al.
Clinical Genetics|April 1, 1983
The fragile X chromosome in a large Indian kindredR J Gardner, R D Smart, J M Cornell, 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 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.
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