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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 RamesarSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|September 24, 1983
Gaucher's disease in the black population of South Africa. A case reportP Jacobs, R Tribe, E M Petersen, et al.The Journal of Clinical Pediatric Dentistry|February 19, 2004
Crouzonodermoskeletal syndromeA Jeftha, L Stephen, J A Morkel, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|December 15, 1984
A clinical and ultrastructural study of osteogenesis imperfecta after flavonoid (Catergen) therapyC J Jones, C Cummings, J Ball, et al.American Journal of Medical Genetics|November 1, 1993
Genetic skeletal dysplasias in the Museum of Pathological Anatomy, ViennaP Beighton, E Sujansky, B Patzak, et al.International Dental Journal|September 26, 2001
Dental and oral manifestations of sclerosteosisL X Stephen, H Hamersma, J Gardner, et al.Human Genetics|July 1, 1997
Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african familiesR S Ramesar, S Bardien, P Beighton, et al.Journal of Medical Genetics|October 1, 1986
Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type IG Wallis, P Beighton, C Boyd, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|November 21, 1987
Morquio's disease type B (beta-galactosidase deficiency) in three siblingsM Beck, E M Petersen, J Spranger, et al.Skeletal Radiology|August 18, 1999
Broad clavicles in trisomy 8 mosaicism: a new signP Beighton, K S Kozlowski, J Gardner, et al.Pageof 24