(Q40504987)

21 September 2017

1 reference

title

Epidemiology of retinitis pigmentosa in the Valencian community (Spain). (English)

1 reference

21 September 2017

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Nájera C

1

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21 September 2017

Millán JM

series ordinal

2

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21 September 2017

Beneyto M

series ordinal

3

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21 September 2017

Prieto F

series ordinal

4

1 reference

21 September 2017

publication date

1 January 1995

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21 September 2017

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21 September 2017

volume

12

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21 September 2017

issue

1

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21 September 2017

page(s)

37-46

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Genetic and epidemiological investigations on pigmentary degeneration of the retina and allied disorders in Switzerland

21 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

Clinical and genetic heterogeneity in retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

Prevalence of retinitis pigmentosa in Maine

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

A retinitis pigmentosa register for Western Australia

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

The ?singles? method for segregation analysis under incomplete ascertainment

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

Retinitis pigmentosa. Genetic percentages

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

Genetic aspects of retinitis pigmentosa in China

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

On the heredity of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

A statistical analysis of the heterogeneity of inherited diseases

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370120105

7 January 2021

Identifiers

DOI

10.1002/GEPI.1370120105

1 reference

release_dibngeftqveljizbuu6fat6iny

21 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dibngeftqveljizbuu6fat6iny

24 November 2022

mapped directly with Wikidata item

1 reference