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Journal of Medical Genetics|June 1, 1993
Edward Meryon (1809-1880) and muscular dystrophyA E Emery, M L EmeryClinica Chimica Acta; International Journal of Clinical Chemistry|April 27, 1981
A possible circulating plasma factor in Duchenne muscular dystrophyS J Lloyd, A E EmeryClinical Genetics|August 1, 1987
Heterogeneity of pseudoxanthoma elasticum: delineation of a new form?D L Viljoen, F M Pope, P BeightonPediatric Radiology|January 9, 1999
Osteochondrodystrophies with marked platyspondyly and distinctive peripheral anomaliesK Kozlowski, T Bieganski, J Gardner, et al.Journal of Medical Genetics|October 1, 1983
Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?D L Viljoen, S L Sellars, P BeightonSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|April 7, 1984
Glucose-6-phosphate dehydrogenase deficiency in the Greek population of Cape TownR P Bonafede, M C Botha, P BeightonClinical Genetics|October 1, 1984
The manifestations and natural history of spondylo-epi-metaphyseal dysplasia with joint laxityP Beighton, G Gericke, K Kozlowski, et al.Clinical Radiology|November 1, 1978
Lethal chondrodysplasia punctataN G Heselson, B J Cremin, P BeightonSkeletal Radiology|January 1, 1982
Wormian bones in osteogenesis imperfecta and other disordersB Cremin, H Goodman, J Spranger, et al.Clinical Genetics|April 29, 2014
Spondyloepimetaphyseal dysplasia with joint laxity (Beighton type); mutation analysis in eight affected South African familiesA A Vorster, P Beighton, R S RamesarPageof 28