(Q34366674)

1 August 2017

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. (English)

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1 August 2017

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C F Inglehearn

1

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1 August 2017

S A Carter

2

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1 August 2017

T J Keen

3

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1 August 2017

J Lindsey

4

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1 August 2017

A M Stephenson

5

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1 August 2017

R Bashir

6

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1 August 2017

M al-Maghtheh

7

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1 August 2017

A T Moore

8

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1 August 2017

M Jay

9

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1 August 2017

A C Bird

10

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1 August 2017

language of work or name

English

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publication date

1 May 1993

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1 August 2017

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1 August 2017

4

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1 August 2017

51-53

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1 August 2017

1

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https://scigraph.springernature.com/pub.10.1038/ng0593-51

1 August 2017

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cites work

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

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

21 January 2018

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Dominant retinitis pigmentosa with reduced penetrance. Further studies of the electroretinogram

21 January 2018

1 reference

Clinical investigation of retinitis pigmentosa

21 January 2018

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7 January 2021

Two forms of autosomal dominant primary retinitis pigmentosa

1 reference

7 January 2021

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

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7 January 2021

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

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7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

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7 January 2021

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa

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7 January 2021

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

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7 January 2021

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

1 reference

7 January 2021

Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRP

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7 January 2021

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

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7 January 2021

Dominant Retinitis Pigmentosa With Reduced Penetrance

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7 January 2021

A 2-cM genetic linkage map of human chromosome 7p that includes 47 loci

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7 January 2021

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

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7 January 2021

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

1 reference

7 January 2021

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

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7 January 2021

Dinucleotide repeat polymorphisms at the D7S435 and D7S440 loci

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7 January 2021

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

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7 January 2021

Strategies for multilocus linkage analysis in humans

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7 January 2021

Identifiers

DOI

10.1038/NG0593-51

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1 August 2017

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