(Q28145835)

English

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)

scientific article (publication date: September 1999)

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title

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2) (English)

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main subject

genotype-phenotype correlation

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retinitis pigmentosa 2

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T Rosenberg

1

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U Schwahn

series ordinal

2

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S Feil

series ordinal

3

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W Berger

series ordinal

4

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language of work or name

English

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publication date

September 1999

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published in

Ophthalmic Genetics

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volume

20

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issue

3

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page(s)

161-72

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cites work

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Positional cloning of the gene for X-linked retinitis pigmentosa 2

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Mutations in the candidate gene for Norrie disease

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Choroido-retinal dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

A genetic linkage study of a kindred with X-linked retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Phenotype-genotype correlations in X linked retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Retinitis pigmentosa: problems associated with genetic classification

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

X-linked retinitis pigmentosa: new map studies of XLRP2, and a possible human centromere effect

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.20.3.161.2278

retrieved

21 January 2018

Identifiers

DOI

10.1076/OPGE.20.3.161.2278

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Fatcat ID

release_zlsakckqmrgkfidja7rj3b26oi

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Fatcat

reference URL

https://api.fatcat.wiki/v0/release/zlsakckqmrgkfidja7rj3b26oi

retrieved

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

10520237

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(Q28145835)

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)

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