Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q (Q71108634)

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16 October 2019

title

Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8643244%20AND%20SRC:MED&resulttype=core&format=json

progressive bifocal chorioretinal atrophy

16 October 2019

main subject

1 reference

B F Godley

1

1 reference

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16 October 2019

P A Tiffin

2

1 reference

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16 October 2019

K Evans

3

1 reference

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16 October 2019

R E Kelsell

4

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16 October 2019

D M Hunt

5

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16 October 2019

A C Bird

6

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16 October 2019

publication date

1 June 1996

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16 October 2019

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16 October 2019

volume

103

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16 October 2019

issue

6

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16 October 2019

page(s)

893-898

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Progressive bifocal chorio-retinal atrophy. A rare familial disease of the eyes

16 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2.

1 reference

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7 January 2021

Distribution of fundus autofluorescence with a scanning laser ophthalmoscope

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7 January 2021

A modified ERG technique and the results obtained in X-linked retinitis pigmentosa

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7 January 2021

Standard for clinical electroretinography. International Standardization Committee

1 reference

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7 January 2021

New clinical test of retinal function based upon the standing potential of the eye.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

North Carolina's dominant progressive foveal dystrophy: how progressive is it?

1 reference

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7 January 2021

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2896%2930590-3

7 January 2021

10.1016/S0161-6420(96)30590-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8643244%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference