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Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter
scientific article (publication date: June 1994)
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
title
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
main subject
fundus dystrophy
1 reference
based on heuristic
inferred from title
Sorsby's fundus dystrophy
1 reference
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inferred from title
author
Bernhard H Weber
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
author name string
Vogt G
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
Wolz W
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
Ives EJ
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
Ewing CC
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
language of work or name
English
0 references
publication date
1 June 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
volume
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
page(s)
158-161
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
cites work
Correlation between biochemical composition and fluorescein binding of deposits in Bruch's membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
21 January 2018
A fundus dystrophy with unusual features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of age-related maculopathy. The Beaver Dam Eye Study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bruch's membrane change with age
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary hemorrhagic macular dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fast and slow oscillations of the electro-oculogram in Best's macular dystrophy and retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Age-related macular degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Choroidal perfusion abnormality with age-related Bruch's membrane change
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sorsby's fundus dystrophy. A light and electron microscopic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Council Lecture. Drusen and their relationship to senile macular degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sorsby's fundus dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exclusion mapping.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integrated human genome-wide maps constructed using the CEPH reference panel.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human interleukin-2 receptor beta-chain gene: genomic organization, promoter analysis and chromosomal assignment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Twelve new polymorphic microsatellites on human chromosome 22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further cases of a fundus dystrophy with unusual features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fluorescein photography of generalized dominant fundus dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary hemorrhagic macular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant macular subretinal neovascularization with peripheral retinal degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pseudoinflammatory Macular Dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sorsby's fundus dystrophy. A clinical study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A second-generation linkage map of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dinucleotide repeat polymorphism in the lL-2Rβ gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0694-158
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0694-158
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
PubMed publication ID
7920634
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7920634
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7920634%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
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