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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.Pediatric Radiology|January 1, 1994
Bone dysplasias of infancy in the Vienna collectionP Beighton, E Sujansky, B Patzak, et al.Clinical Orthopaedics and Related Research|March 1, 1984
Collagen defect of bone in osteogenesis imperfecta (Type I). An electron microscopic studyC J Jones, C Cummings, J Ball, et al.Journal of Medical Genetics|April 1, 1982
Apparent enhanced response to the induction of sister chromatid exchange by mitomycin C in myotonic dystrophyVijayalaxmi, A E Emery, H J EvansThe Journal of Clinical Pediatric Dentistry|February 19, 2004
Dental implications of Tooth-Nail dysplasia (Witkop syndrome): a report of an affected family and an approach to dental managementG M Wicomb, L X G Stephen, P BeightonClinical Genetics|May 1, 1979
A study of possible heterogeneity in Duchenne muscular dystrophyA E Emery, R Skinner, S HollowaySouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|December 19, 1987
Duchenne muscular dystrophy in South Africa. Prevention by molecular techniquesJ Goldblatt, R Ballo, G Wallis, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|September 6, 1980
Sclerosteosis in old ageA H Barnard, H Hamersma, J H Kretzmar, et al.Pageof 28