(Q35716618)

9 August 2017

1 reference

title

Molecular genetics of inherited retinal degenerations (English)

1 reference

9 August 2017

1 reference

Lindsay S

1

1 reference

9 August 2017

Inglehearn CF

series ordinal

2

1 reference

9 August 2017

Curtis A

series ordinal

3

1 reference

9 August 2017

Bhattacharya S

series ordinal

4

1 reference

9 August 2017

1 June 1992

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Current Opinion in Genetics & Development

9 August 2017

1 reference

9 August 2017

2

1 reference

9 August 2017

459-466

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9 August 2017

3

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X-linked retinitis pigmentosa

9 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Clinical investigation of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Localization of Usher syndrome type II to chromosome 1q.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1q

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Non-allelic mutations in X-linked retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Report of the committee on the genetic constitution of the X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Aland eye disease: no albino misrouting

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Linkage analysis in X-linked ocular albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Cloning of a gene that is rearranged in patients with choroideraemia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Pathology of Hereditary Juvenile Retinoschisis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Refined localization of the gene causing X-linked juvenile retinoschisis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980158-3

7 January 2021

10.1016/S0959-437X(05)80158-3

Identifiers

DOI

1 reference

9 August 2017

1 reference