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Clinical Genetics|March 1, 1979
Craniometaphyseal dysplasia--variability of expression within a large familyP Beighton, H Hamersma, F HoranClinical Genetics|August 1, 1989
Osteogenesis imperfecta with congenital joint contractures (Bruck syndrome)D Viljoen, G Versfeld, P BeightonAnnals 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 BeightonAmerican Journal of Medical Genetics|December 1, 1984
X-linked inheritance of ocular albinism with late-onset sensorineural deafnessI Winship, G Gericke, P BeightonClinical Genetics|February 1, 1984
Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafnessJ Cornell, S Sellars, P BeightonPageof 23