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English
The gene for an inherited form of deafness maps to chromosome 5q31
scientific article published on June 1, 1992
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
title
The gene for an inherited form of deafness maps to chromosome 5q31
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
main subject
human chromosome 5
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
deafness
1 reference
based on heuristic
inferred from title
author
Mary-Claire King
series ordinal
5
object named as
M. C. King
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
author name string
P. E. Leon
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
H. Raventos
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
E. Lynch
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
J. Morrow
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
language of work or name
English
0 references
publication date
1 June 1992
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
full work available at URL
https://europepmc.org/articles/PMC49253
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
https://europepmc.org/articles/PMC49253?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1350680
retrieved
17 September 2022
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
volume
89
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
issue
11
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
page(s)
5181-5184
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
cites work
The gene for Treacher Collins syndrome maps to the long arm of chromosome 5
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=49253
retrieved
24 March 2017
"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum
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=49253
retrieved
24 March 2017
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
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=49253
retrieved
24 March 2017
Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3
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=49253
retrieved
24 March 2017
Radiation hybrid map of 13 loci on the long arm of chromosome 5
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=49253
retrieved
24 March 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=49253
retrieved
7 April 2017
Low frequency hereditary deafness in man with childhood onset
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=49253
retrieved
27 September 2017
Oncogenes and human breast cancer
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=49253
retrieved
27 September 2017
Report of the chromosome 5 workshop
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=49253
retrieved
27 September 2017
Dinucleotide repeat polymorphism at the human interleukin 9 gene
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=49253
retrieved
27 September 2017
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin 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=49253
retrieved
27 September 2017
A novel approach to establishing permanent lymphoblastoid cell lines: Epstein-Barr virus transformation of cryopreserved lymphocytes
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=49253
retrieved
30 May 2018
Mapping of human chromosome 5 microsatellite DNA polymorphisms
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1350680
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.89.11.5181
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
ADS bibcode
1992PNAS...89.5181L
0 references
Fatcat ID
release_yskgmgeeljh4nnkbxjasg7nkna
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/yskgmgeeljh4nnkbxjasg7nkna
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PMCID
49253
0 references
PubMed ID
1350680
1 reference
stated in
Europe PubMed Central
PubMed ID
1350680
retrieved
23 June 2017
ResearchGate publication ID
21804390
0 references
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