Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness

Author:

Boycott Kym M.,Pearce William G.,Musarella Maria A.,Weleber Richard G.,Maybaum Tracy A.,Birch David G.,Miyake Yozo,Young Rockefeller S.L.,Bech-Hansen N. Torben

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference52 articles.

1. Linkage analysis in X-linked congenital stationary night blindness;Aldred;Genomics,1992

2. Localization of the Åland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis;Alitalo;Am J Hum Genet,1991

3. 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

4. Localization of CSNB1 to region Xp11.3-Xp11.22 proximal to MAOA, B, Human Gene Mapping 11;Bech-Hansen;Cytogenet Cell Genet,1991

5. Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7;Bech-Hansen;Genomics,1992

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