Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24681273)
Watch
English
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q
scientific article
In more languages
edit
Statements
instance of
scholarly article
0 references
title
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q
(English)
0 references
main subject
heterogeneity
1 reference
based on heuristic
inferred from title
Usher syndrome
1 reference
based on heuristic
inferred from title
author name string
S Pieke-Dahl
series ordinal
1
0 references
C G Möller
series ordinal
2
0 references
P M Kelley
series ordinal
3
0 references
L M Astuto
series ordinal
4
0 references
C W Cremers
series ordinal
5
0 references
M B Gorin
series ordinal
6
0 references
W J Kimberling
series ordinal
7
0 references
language of work or name
English
0 references
publication date
April 2000
0 references
published in
Journal of Medical Genetics
0 references
volume
37
0 references
page(s)
256-62
0 references
issue
4
0 references
cites work
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
7 April 2017
Isolation, characterization, and chromosomal localization of mouse and human COUP-TF I and II genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
7 April 2017
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
7 April 2017
Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
7 April 2017
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
7 April 2017
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 September 2017
Genetic heterogeneity of Usher syndrome type II in a Dutch population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 September 2017
Genetic heterogeneity of Usher syndrome type II
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 September 2017
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 September 2017
Chicken ovalbumin upstream promoter transcription factor (COUP-TF): expression during mouse embryogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 September 2017
Hearing impairment related to age in Usher syndrome types 1B and 2A.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
30 May 2018
Stable and progressive hearing loss in type 2A Usher's syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
30 May 2018
Usher syndrome: an otoneurologic study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
30 May 2018
Progressive hearing loss in Usher's syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
30 May 2018
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 November 2018
Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 November 2018
Clinical and molecular genetics of Usher syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 November 2018
Heterogeneity of retinal degeneration and hearing impairment syndromes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734554
retrieved
28 November 2018
Identifiers
DOI
10.1136/JMG.37.4.256
0 references
PMCID
1734554
0 references
PubMed ID
10745043
0 references
ResearchGate publication ID
277389429
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit