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Localizing Multiple X Chromosome-Linked Retinitis Pigmentosa Loci Using Multilocus Homogeneity Tests

Proceedings of the National Academy of Sciences - PNAS, 1990-01, Vol.87 (2), p.701-704

1990

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Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease

Investigative ophthalmology & visual science, 2012-12, Vol.53 (13), p.8232-8237

2012

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Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older

Ophthalmology (Rochester, Minn.), 1999-09, Vol.106 (9), p.1780-1785

1999

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A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis Pigmentosa

American journal of human genetics, 2002-06, Vol.70 (6), p.1545-1554

2002

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A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa

Ophthalmology (Rochester, Minn.), 2000-02, Vol.107 (2), p.386-396

2000

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Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

American journal of human genetics, 1997-12, Vol.61 (6), p.1287-1292

1997

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Visual Acuity Impairment in Patients with Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 1996-10, Vol.103 (10), p.1593-1600

1996

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Rhodopsin Mutations in Autosomal Dominant Retinitis Pigmentosa

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (15), p.6481-6485

1991

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Five novel RPGR mutations in families with X-linked retinitis pigmentosa

Human mutation, 2001-02, Vol.17 (2), p.151-151

2001

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Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families

Genomics (San Diego, Calif.), 1990-10, Vol.8 (2), p.286-296

1990

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A genetic analysis of retinitis pigmentosa

British journal of ophthalmology, 1983-07, Vol.67 (7), p.449-454

1983

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X-linked retinitis pigmentosa. Profile of clinical findings

Archives of ophthalmology (1960), 1988-03, Vol.106 (3), p.369

1988

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Retinitis pigmentosa. Genetic percentages

Archives of ophthalmology (1960), 1978-05, Vol.96 (5), p.822

Fishman, G A

1978

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X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers

Archives of ophthalmology (1960), 1986-09, Vol.104 (9), p.1329

1986

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Retinitis pigmentosa. Visual loss

Archives of ophthalmology (1960), 1978-07, Vol.96 (7), p.1185

Fishman, G A

1978

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Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype

Archives of ophthalmology (1960), 1985-04, Vol.103 (4), p.524

1985

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A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

Nature genetics, 1996-05, Vol.13 (1), p.35-42

1996

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Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa

British journal of ophthalmology, 1999-10, Vol.83 (10), p.1144-1148

1999

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Localization of two genes for usher syndrome type I to chromosome 11

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.995-1002

1992

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On the heredity of retinitis pigmentosa

British journal of ophthalmology, 1982-07, Vol.66 (7), p.405-416

Jay, M.

1982

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Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q

British journal of ophthalmology, 1995-09, Vol.79 (9), p.841-846

1995

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Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records

Journal of medical genetics, 1992-12, Vol.29 (12), p.906-910

1992

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Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study

British journal of ophthalmology, 1993-08, Vol.77 (8), p.473-479

1993

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Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression

British journal of ophthalmology, 1995-01, Vol.79 (1), p.23-27

1995

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no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneity

Genomics (San Diego, Calif.), 1990, Vol.6 (1), p.168-173

1990

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Localizing Multiple X Chromosome-Linked Retinitis Pigmentosa Loci Using Multilocus Homogeneity Tests

Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease

Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older

A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis Pigmentosa

A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa

Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

Visual Acuity Impairment in Patients with Retinitis Pigmentosa

Rhodopsin Mutations in Autosomal Dominant Retinitis Pigmentosa

Five novel RPGR mutations in families with X-linked retinitis pigmentosa

Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families

A genetic analysis of retinitis pigmentosa

X-linked retinitis pigmentosa. Profile of clinical findings

Retinitis pigmentosa. Genetic percentages

X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers

Retinitis pigmentosa. Visual loss

Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa

Localization of two genes for usher syndrome type I to chromosome 11

On the heredity of retinitis pigmentosa

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q

Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study

Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression

no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneity

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