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Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype

published in: American Journal of Human Genetics

date of publication: 1996-10

language: English

main subject: retinitis pigmentosa

Cites articles 25

Date

Title

Authors

1996-02-01

Nomenclature for inherited diseases of the retina
1995-08

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q

Soraya Bardien, Rajkumar Ramesar
1995-11-01

Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family

Mitsuru Nakazawa
1995-01-01

Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression
1995-09-01

When more is less: pathogenesis of glutamine repeat neurodegenerative diseases
1995-09-01

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

Geoffrey Arden
1994-02

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion
1994-02

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19
1994-06

The 1993-94 Généthon human genetic linkage map,The 1993–94 Généthon human genetic linkage map

Jean Weissenbach, Mark Lathrop, Cécile Fizames, Gabor Gyapay
1994-06-01

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
1994-06-01

A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.
1993-05-01

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.
1993-08-01

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study
1993-05-01

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

Carmen Ayuso, Javier Benitez
1992-04-01

The UK Human Genome Mapping Project online computing service

Martin J. Bishop, Gareth W. Williams
1991-12-12

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa,A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa
1991-12-12

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
1991-12-01

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Stephen P. Daiger
1990-01-01

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Glenn S Cowley
1988-07-01

A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors
1985-05-01

A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa
1984-06

Strategies for multilocus linkage analysis in humans

Mark Lathrop, Jean-Marc Lalouel
1984-03-01

Easy calculations of lod scores and genetic risks on small computers

Mark Lathrop, Jean-Marc Lalouel
1982-01-01

Figures and fantasies: the frequencies of the different genetic forms of retinitis pigmentosa
1980-03-01

Population genetic studies of retinitis pigmentosa

Article - wd:Q24675745

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