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English
Selection for deafness?
scientific article published on 01 December 2002
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
title
Selection for deafness?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
main subject
deafness
1 reference
based on heuristic
inferred from title
author name string
Christian G Meyer
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Geoffrey K Amedofu
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Johanna M Brandner
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Dieter Pohland
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Christian Timmann
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Rolf D Horstmann
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
publication date
1 December 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
published in
Nature Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
volume
8
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
issue
12
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
page(s)
1332-1333
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/nm1202-1332
0 references
cites work
What maintains the frequencies of human genetic diseases?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Advances in hereditary deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High carrier frequency of the 35delG deafness mutation in European populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Upregulation of connexin 26 between keratinocytes of psoriatic lesions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalent connexin 26 gene (GJB2) mutations in Japanese
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM1202-1332
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NM1202-1332
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
Dimensions Publication ID
1043277212
0 references
PubMed ID
12457154
1 reference
stated in
Europe PubMed Central
PubMed ID
12457154
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12457154%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 December 2019
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