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Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|May 26, 2009
Klippel-Trenaunay-Weber syndrome: orodental manifestations and management considerationsEbrahim Fakir, Tina Roberts, Lawrence Stephen, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 27, 2016
A clinical and molecular investigation of two South African families with Simpson-Golabi-Behmel syndromeCareni Spencer, Karen Fieggen, Anna Vorster, et al.
Clinical Dysmorphology|June 20, 2002
Lethal non-rhizomelic dysplasia epiphysealis punctataKazimierz Kozlowski, John Godlonton, Jessica Gardner, et al.
American Journal of Human Genetics|August 5, 2005
A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritisLindsay Gleghorn, Rajkumar Ramesar, Peter Beighton, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 27, 2016
Digitotalar dysmorphism: Molecular elucidationAnna Alvera Vorster, Peter Beighton, Rajkumar Sewcharan Ramesar
Archives of Neurology|November 15, 2006
Stroke caused by human immunodeficiency virus-associated intracranial large-vessel aneurysmal vasculopathyBrent Tipping, Linda de Villiers, Sally Candy, et al.
BDJ Open|April 3, 2018
Craniofacial manifestations in osteogenesis imperfecta type III in South AfricaManogari Chetty, Tina Sharon Roberts, Lawrence Stephen, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|May 4, 2016
Syphilitic lymphadenitis clinically and histologically mimicking lymphogranuloma venereumAnnesu Wessels, Colleen Bamford, David Lewis, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|December 21, 2010
Fibrodysplasia ossificans progressiva in South Africa: difficulties in management in a developing countryChris Scott, Mike Urban, Regan Arendse, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Arterial rupture in classic Ehlers-Danlos syndrome with COL5A1 mutationGuntram Borck, Peter Beighton, Christian Wilhelm, et al.
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