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A novel mutation, Ala315Ser, in FGFR2: a gene–environment interaction leading to craniosynostosis?
article
A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
title
A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
main subject
craniosynostosis
0 references
author
Andrew Oliver Mungo Wilkie
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
author name string
Johnson D
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
Wall SA
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
Mann S
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
language of work or name
English
0 references
publication date
1 August 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
published in
European Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
volume
8
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
page(s)
571-577
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
issue
8
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
exact match
https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200499
0 references
Identifiers
DOI
10.1038/SJ.EJHG.5200499
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
PubMed ID
10951518
1 reference
stated in
Europe PubMed Central
PubMed ID
10951518
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10951518%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
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