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Article

X-linked retinitis pigmentosa: report of a large kindred with loss of central vision and preserved peripheral function.

American journal of medical genetics - 20 Nov 1995

Shastry B S, Trese M T

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PMID: 8599373
DOI: 10.1002/ajmg.1320590329

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X-linked retinitis pigmentosa: report of a large kindred with loss of central vision and preserved peripheral function.PMID 8599373Read ↗

RPGR: part one of the X-linked retinitis pigmentosa story.Semantic proximity Read ↗

A novel locus for X-linked retinitis pigmentosa.Semantic proximity Read ↗

X-Linked Retinoschisis without Macular Retinoschisis: A New RS1 Mutation.Semantic proximity Read ↗

An unusual fundus phenotype of inner retinal sheen in X-linked retinoschisis.Semantic proximity Read ↗

X-linked peripheral retinoschisis without macular involvement: a case series with RS1 genetic confirmation.Semantic proximity Read ↗

X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype.Semantic proximity Read ↗

Severe Phenotypic Presentation of RPGR-associated X-linked Retinitis Pigmentosa in Female Carriers: Two Case Reports.Semantic proximity Read ↗

Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.Semantic proximity Read ↗

Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree.Semantic proximity Read ↗

A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalitiesSemantic proximity Read ↗

The first reported case of a deletion of the entire RPGR gene in a family with X-linked retinitis pigmentosa.Semantic proximity Read ↗

Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype.Semantic proximity Read ↗

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