Localization of a Novel X-Linked Progressive Cone Dystrophy Gene to Xq27: Evidence for Genetic Heterogeneity
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (XJ1.1) and is linked to DXS84 (754);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 in X-linked ocular albinism of the Net-tleship-Falls type;Bergen;Hum Genet,1991
4. Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential ALL PCR fingerprint cloning;Bergen;Cytogenet Cell Genet,1993
5. Congenital X-linked incomplete achromatopsia: evidence for slow progression, carrier fundus findings, and possible genetic linkage with the G6PD locus;Fleischman;Arch Ophthalmol,1981
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