Linkage Analysis of X-linked Cone-Rod Dystrophy: Localization to Xp11.4 and Definition of a Locus Distinct from RP2 and RP3

Author:

Seymour Albert B.,Dash-Modi Anita,O'Connell Jeffrey R.,Shaffer-Gordon Maria,Mah Tammy S.,Stefko S. Tonya,Nagaraja Ramaiah,Brown Jeremiah,Kimura Alan E.,Ferrell Robert E.,Gorin Michael B.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (Xj1.1) and is linked to DXS84;Bartley;Cytogenet Cell Genet,1989

2. Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3;Bergen;Genomics,1993

3. Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families;Bergen;Ophthalmic Genet,1995

4. Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci;Chen;Am J Hum Genet,1989

5. A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy;Chen;Nat Genet,1993

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