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Clinical Genetics|June 1, 1990
Marfan syndrome: a diagnostic dilemmaD Viljoen, P Beighton
Journal of Medical Genetics|January 1, 1992
Schwartz-Jampel syndrome (chondrodystrophic myotonia)D Viljoen, P Beighton
American Journal of Medical Genetics|January 1, 1991
Epiphyseal stippling in acrodysostosisD Viljoen, P Beighton
American Journal of Medical Genetics|August 1, 1987
Osteogenesis imperfecta type III: an ancient mutation in Africa?D Viljoen, P Beighton
Clinical Genetics|August 1, 1989
Osteogenesis imperfecta with congenital joint contractures (Bruck syndrome)D Viljoen, G Versfeld, P Beighton
Clinical Genetics|August 1, 1984
Manifestations and natural history of idiopathic hemihypertrophy: a review of eleven casesD Viljoen, J Pearn, P Beighton
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|November 26, 1983
Limb overgrowth--clinical observations and nosological considerationsJ Pearn, D Viljoen, P Beighton
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 1, 1994
Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affectedR Ballo, D Viljoen, P Beighton
Clinical Genetics|September 1, 1987
Ehlers-Danlos syndrome: yet another type?D Viljoen, J Goldblatt, D Thompson, et al.
American Journal of Medical Genetics|July 1, 1993
Brachydactylous dwarfs of MseleniD Viljoen, V Fredlund, R Ramesar, et al.
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