Showing results (181-190 of 225) with videos related to

Sort By:
Pageof 23
Clinical Genetics|October 1, 1986
St. Helena familial genu valgumP Beighton, H S Myers, S J Aldridge, et al.
American Journal of Medical Genetics|December 31, 1997
Mseleni and Handigodu familial osteoarthropathies: syndromic identity?S S Agarwal, S R Phadke, V Fredlund, et al.
American Journal of Human Genetics|March 1, 1991
Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1C Sher, R Ramesar, R Martell, et al.
American Journal of Medical Genetics|April 29, 1998
Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK)P Beighton, A De Paepe, B Steinmann, et al.
Clinical Genetics|May 1, 1991
Piebaldism: an autonomous autosomal dominant entityI Winship, K Young, R Martell, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 1, 1987
Childhood deafness in the Indian population of NatalP Beighton, S L Sellars, J Goldblatt, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|November 24, 1984
Pseudoxanthoma elasticum in South Africa--genetic and clinical implicationsD L Viljoen, P Beighton, T Mabin, et al.
American Journal of Human Genetics|June 7, 2000
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27P Ianakiev, M W Kilpatrick, I Toudjarska, et al.
The British Journal of Radiology|June 1, 1979
The radiological manifestations of metaphyseal dysplasia (Pyle disease)N G Heselson, M S Raad, H Hamersma, et al.
Clinical Genetics|April 1, 1983
The fragile X chromosome in a large Indian kindredR J Gardner, R D Smart, J M Cornell, et al.
Pageof 23