1-11 of 11
Authors: Alan C. Bird
Journal Article
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB–FKBPL–NOTCH4 region of chromosome 6p21.3 Get access
Human Molecular Genetics, Volume 21, Issue 18, 15 September 2012, Pages 4138–4150, https://doi.org/10.1093/hmg/dds225
Published: 13 June 2012
Journal Article
Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa Get access
Human Molecular Genetics, Volume 11, Issue 1, 1 January 2002, Pages 87–92, https://doi.org/10.1093/hmg/11.1.87
Published: 01 January 2002
Journal Article
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13) Get access
Human Molecular Genetics, Volume 10, Issue 15, 15 July 2001, Pages 1555–1562, https://doi.org/10.1093/hmg/10.15.1555
Published: 15 July 2001
Journal Article
Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy Get access
Human Molecular Genetics, Volume 7, Issue 7, July 1998, Pages 1179–1184, https://doi.org/10.1093/hmg/7.7.1179
Published: 01 July 1998
Journal Article
A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1 Get access
Human Molecular Genetics, Volume 7, Issue 2, February 1998, Pages 273–277, https://doi.org/10.1093/hmg/7.2.273
Published: 01 February 1998
Journal Article
Localisation of a Gene for Dominant Cone-Rod Dystrophy (CORD6) to Chromosome 17p Get access
Human Molecular Genetics, Volume 6, Issue 4, 1 April 1997, Pages 597–600, https://doi.org/10.1093/hmg/6.4.597
Published: 01 April 1997
Journal Article
The Gene Responsible for Autosomal Dominant Doyne's Honeycomb Retinal Dystrophy (DHRD) Maps to Chromosome 2p16 Get access
Human Molecular Genetics, Volume 5, Issue 7, 1 July 1996, Pages 1055–1059, https://doi.org/10.1093/hmg/5.7.1055
Published: 01 July 1996
Journal Article
Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3) Get access
Human Molecular Genetics, Volume 4, Issue 12, December 1995, Pages 2347–2353, https://doi.org/10.1093/hmg/4.12.2347
Published: 01 December 1995
Journal Article
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q Get access
Human Molecular Genetics, Volume 4, Issue 9, September 1995, Pages 1653–1656, https://doi.org/10.1093/hmg/4.9.1653
Published: 01 September 1995
Journal Article
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19 Get access
Human Molecular Genetics, Volume 3, Issue 2, February 1994, Pages 351–354, https://doi.org/10.1093/hmg/3.2.351
Published: 01 February 1994
Journal Article
Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin geneother Get access
Human Molecular Genetics, Volume 3, Issue 2, February 1994, Pages 367–368, https://doi.org/10.1093/hmg/3.2.367
Published: 01 February 1994
