Linkage analysis in X-linked congenital stationary night blindness
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference20 articles.
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2. A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome;Bech-Hansen;Hum. Genet.,1990
3. Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7;Bech-Hansen;Genomics,1992
4. Dinucleotide repeat polymorphism at the MAOA locus;Black;Nucleic Acids Res.,1991
5. Dinucleotide repeat polymorphism at the DXS538 locus;Browne;Nucleic Acids Res.,1991
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1. Retinitis Pigmentosa and Allied Disorders;Retina;2006
2. Genotype-phenotype correlation in British families with X linked congenital stationary night blindness;British Journal of Ophthalmology;2003-11-01
3. Mutations in theCACNA1F andNYX genes in British CSNBX families;Human Mutation;2003-01-27
4. Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family;European Journal of Human Genetics;1999-06-22
5. UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2;European Journal of Human Genetics;1998-09
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