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Case Reports in Genetics
Volume 2012 (2012), Article ID 136582, 3 pages
doi:10.1155/2012/136582
Sickle Retinopathy in a Person with Hemoglobin S/New York Disease
1Department of Surgery, Radiology, Anaesthetics, and Intensive Care, Faculty of Medical Sciences, University of the West Indies, Mona, Kingston 7, Jamaica
2Universite des Antilles et de la Guyane, Centre Hospitalier Universitaire (CHU), Pointe-a-Pitre, UMR S 458 Inserm, 97159 Guadeloupe, France
3Inserm U763, Pointe-à-Pitre, 97159 Guadeloupe, France
4Université des Antilles et de la Guyane, 97159 Guadeloupe, France
5Sickle Cell Unit, Tropical Medicine Research Institute, University of the West Indies, Mona, Kingston 7, Jamaica
Received 30 November 2012; Accepted 19 December 2012
Academic Editors: S. Chappell and M. Velinov
Copyright © 2012 Donovan Calder et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
How to Cite this Article
Donovan Calder, Maryse Etienne-Julan, Marc Romana, Naomi Watkins, and Jennifer M. Knight-Madden, “Sickle Retinopathy in a Person with Hemoglobin S/New York Disease,” Case Reports in Genetics, vol. 2012, Article ID 136582, 3 pages, 2012. doi:10.1155/2012/136582