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Clinical Dysmorphology|July 1, 1995
A case of lateral facial cleft, cleft lip and palate, anophthalmia, microtia, clavicular agenesis and asterniaG Samson, D ViljoenAmerican Journal of Medical Genetics|December 1, 1994
Aplasia cutis congenita with epibulbar dermoids: further evidence for syndromic identity of the ocular ectodermal syndromeJ Gardner, D ViljoenAmerican Journal of Medical Genetics|November 1, 1987
New autosomal dominant radial ray hypoplasia syndromeJ Goldblatt, D ViljoenClinical Genetics|March 1, 1979
Craniometaphyseal dysplasia--variability of expression within a large familyP Beighton, H Hamersma, F HoranAnnals of Internal Medicine|April 1, 1976
The clinical features of sclerosteosis. A review of the manifestations in twenty-five affected individualsP Beighton, L Durr, H HamersmaClinical Genetics|September 1, 1979
Oculodento-osseous dysplasia: heterogeneity or variable expression?P Beighton, H Hamersma, M RaadSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 30, 1979
Endocrine function in sclerosteosisS Epstein, H Hamersma, P BeightonSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|July 5, 1975
Childhood deafness in Cape TownS Sellars, E Napier, P BeightonArchives of Disease in Childhood|September 1, 1979
Non-neuropathic Gaucher disease presenting in infancyP Hodson, J Goldblatt, P BeightonAustralasian Radiology|February 28, 2006
Retrospective diagnosis of chondrodysplasia punctataK Kozlowski, D Basel, P BeightonPageof 26