Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference14 articles.
1. A genetic analysis of retinitis pigmentosa.
2. , , (1989): Exclusion of the autosomal dominant retinitis pigmentosa gene from a substantial region of chromosome 1: study of a large Australian family. Aust NZ J Ophthalmol (in press).
3. Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7
4. Autosomal Dominant Retinitis Pigmentosa
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1. Molecular Genetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2010-09-24
2. Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease;Clinical Genetics;2008-06-28
3. Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin;Clinical Genetics;2008-06-28
4. Retinitis pigmentosa and related disorders: Phenotypes of rhodopsin and peripherin/RDS mutations;American Journal of Medical Genetics;1994-10-01
5. Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa;Genomics;1993-07
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