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Deafness locus DFNB16 is located on chromosome 15q13-q21 within a 5-cM interval flanked by markers D15S994 and D15S132
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
title
Deafness locus DFNB16 is located on chromosome 15q13-q21 within a 5-cM interval flanked by markers D15S994 and D15S132
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
main subject
deafness
1 reference
based on heuristic
inferred from title
author
Ignacio del Castillo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
author name string
M Villamar
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
N Valle
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
L Romero
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
F Moreno
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
language of work or name
English
0 references
publication date
1 April 1999
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
volume
64
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
page(s)
1238-1241
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
cites work
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F302321
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F302321
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F302321
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F302321
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F302321
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., Canada.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1086%2F302321
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1086/302321
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
PMCID
1377853
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
PubMed ID
10090914
1 reference
stated in
Europe PubMed Central
PMCID
1377853
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090914%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 November 2019
ResearchGate publication ID
238300790
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