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Online Mendelian Inheritance in Man
Online Mendelian Inheritance in Man
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312700 Detailed references and genetic information on Retinoschisis. The NCBI web site requires JavaScript to function. Biotechnology Information Welcome to NCBI The National Center for Biotechnology Information advances science and health by providing access to biomedical and genomic information. NLM/NCBI H1N1 Flu Resources NCBI will be responsible forwaiting for hand_moderation OMIM, RETINOSCHISIS, 1, X, LINKED, JUVENILE, RS1 Retina > Retinoschisis
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Other links at Retina > Retinoschisis
Summarizes the known facts about the disease.
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From Wikipedia, the free encyclopedia Classification and external resources disease characterized by the abnormal splitting of the 's neurosensory layers, usually in the , resulting in a loss of vision in the corresponding visual field in some rarer forms. More common forms are usually
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2. RS links
Jon Diercks's links about X-Linked Recessive Juvenile Retinoschisis.
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X-Linked Recessive Juvenile Retinoschisis (RS) Retinoschisis causes the layers of the retina to separate from each other, distorting the visual image in such a way that it cannot be at the National Organization for Rare Disorders (NORD) RS is passed from parent to child via a recessive gene on
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Detailing signs and symptoms and pathophysiology.
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The page you are looking for might have been removed, had its name changed, or is temporarily unavailable. Please try the following: Make sure that the Web site address displayed in the address bar of your browser is spelled and formatted correctly. If you reached this page by clicking a link,
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Helth. Eye Disorders Directory.
Helth. Eye Disorders Directory.