Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3

[1] Bellingham J, 1997, DEGENERATIVE RETINAL DISEASES, P295

[2] A comprehensive genetic map of the human genome based on 5,264 microsatellites [J]. NATURE, 1996, 380 (6570) : 152 - 154

[3] ELSTON J, 1992, PAEDIAT OPHTHALMOLOG, P3

[4] GENETIC-LINKAGE OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME 19Q AND EVIDENCE FOR SEGREGATION DISTORTION [J]. NATURE GENETICS, 1994, 6 (02) : 210 - 213

[5] CHROMOSOME 19Q CONE-ROD RETINAL DYSTROPHY - OCULAR PHENOTYPE [J]. ARCHIVES OF OPHTHALMOLOGY, 1995, 113 (02) : 195 - 201

[6] Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor [J]. CELL, 1997, 91 (04) : 543 - 553

[7] Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region but splice defects in two families [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (03) : 571 - 580

[8] Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation [J]. CELL, 1997, 91 (04) : 531 - 541

[9] GREGORY CY, 1994, AM J HUM GENET, V55, P1061

[10] YEAST ARTIFICIAL CHROMOSOME LIBRARIES CONTAINING LARGE INSERTS FROM MOUSE AND HUMAN DNA [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (10) : 4123 - 4127

[1] Bellingham J, 1997, DEGENERATIVE RETINAL DISEASES, P295

[2] A comprehensive genetic map of the human genome based on 5,264 microsatellites [J]. NATURE, 1996, 380 (6570) : 152 - 154

[3] ELSTON J, 1992, PAEDIAT OPHTHALMOLOG, P3

[4] GENETIC-LINKAGE OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME 19Q AND EVIDENCE FOR SEGREGATION DISTORTION [J]. NATURE GENETICS, 1994, 6 (02) : 210 - 213

[5] CHROMOSOME 19Q CONE-ROD RETINAL DYSTROPHY - OCULAR PHENOTYPE [J]. ARCHIVES OF OPHTHALMOLOGY, 1995, 113 (02) : 195 - 201

[6] Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor [J]. CELL, 1997, 91 (04) : 543 - 553

[7] Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region but splice defects in two families [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (03) : 571 - 580

[8] Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation [J]. CELL, 1997, 91 (04) : 531 - 541

[9] GREGORY CY, 1994, AM J HUM GENET, V55, P1061

[10] YEAST ARTIFICIAL CHROMOSOME LIBRARIES CONTAINING LARGE INSERTS FROM MOUSE AND HUMAN DNA [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (10) : 4123 - 4127