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Ophthalmic Genetics Volume 23, 2002 - Issue 1
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Research Article

A computer-based register for inherited retinal dystrophies in Southern Africa

M.T. Rebello Division of Human Genetics, UCT Medical School, Observatory, South Africa
,
L.J. Greenberg Division of Human Genetics, UCT Medical School, Observatory, South Africa
&
R.S. Ramesar Division of Human Genetics, UCT Medical School, Observatory, South Africa
Pages 61-65 | Published online: 08 Jul 2009

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Beatrice Bocquet, Annie Lacroux, Marie-Odile Surget, Corinne Baudoin, Virginie Marquette, Gael Manes, Maxime Hebrard, Audrey Sénéchal, Cecile Delettre, Anne-Francoise Roux, Mireille Claustres, Claire-Marie Dhaenens, Jean-Michel Rozet, Isabelle Perrault, Jean-Paul Bonnefont, Josseline Kaplan, Helene Dollfus, Patrizia Amati-Bonneau, Dominique Bonneau, Pascal Reynier, Isabelle Audo, Christina Zeitz, José Alain Sahel, Veronique Paquis-Flucklinger, Patrick Calvas, Benoit Arveiler, Suzanne Kohl, Bernd Wissinger, Catherine Blanchet, Isabelle Meunier & Christian P. Hamel. (2013) Relative Frequencies of Inherited Retinal Dystrophies and Optic Neuropathies in Southern France: Assessment of 21-year Data Management. Ophthalmic Epidemiology 20:1, pages 13-25.
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Articles from other publishers (4)

Caroline Atef Tawfik, Maged Maher Roshdy & Nancy Magdy Morris. (2023) Prevalence of inherited retinal diseases in a large Egyptian cohort. BMC Ophthalmology 23:1.
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Lisa Roberts, Stephanie Julius, Shrinav Dawlat, Safiye Yildiz, George Rebello, Surita Meldau, Komala Pillay, Alina Esterhuizen, Alvera Vorster, Gameda Benefeld, Jorge Rocha, Peter Beighton, Sean L. Sellars, Kebashni Thandrayen, John M. Pettifor & Raj S. Ramesar. (2020) Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B . Human Mutation 41:11, pages 1871-1876.
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Lisa Roberts, George Rebello, Jacquie Greenberg & Raj Ramesar. 2019. Retinal Degenerative Diseases. Retinal Degenerative Diseases 257 261 .
G Rebello, A Vorster, J Greenberg, N Coutts, L Roberts, L Ehrenreich, D Gama & R Ramesar. (2003) Analysis of RPGR in a South African family with X-linked retinitis pigmentosa: research and diagnostic implications. Clinical Genetics 64:2, pages 137-141.
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