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Journal of Medical Genetics|June 1, 1979
Inherited anaemias in the Greek community of Cape TownR P Bonafede, M C Botha, P BeightonClinical Genetics|January 1, 1977
Sclerosteosis - an autosomal recessive disorderP Beighton, J Davidson, L Durr, et al.American Journal of Medical Genetics|July 1, 1993
Brachydactylous dwarfs of MseleniD Viljoen, V Fredlund, R Ramesar, et al.Clinical Genetics|May 1, 1989
Radial ray defects and associated anomaliesH Cox, D Viljoen, G Versfeld, et al.Clinical Genetics|June 1, 1992
Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British originJ Greenberg, M Babaya, R Ramesar, et al.Clinical Orthopaedics and Related Research|March 1, 1988
Total hip arthroplasty in Gaucher's disease. Long-term prognosisJ Goldblatt, S Sacks, D Dall, et al.Clinical Genetics|January 1, 1987
Heterozygous manifestations of Langer mesomelic dysplasiaJ Goldblatt, C Wallis, D Viljoen, et al.Clinical Radiology|January 1, 1979
The radiographic manifestations of hypochondroplasiaN G Heselson, B J Cremin, P BeightonSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 11, 1986
A microcomputer-based relational database for an academic department of human geneticsF van Greunen, K J MacGregor, P BeightonHuman Molecular Genetics|June 1, 1994
A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17J Greenberg, R Goliath, P Beighton, et al.Pageof 24