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English
Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease
scientific article published on 01 December 2010
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
title
Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
main subject
congenital heart disease
1 reference
based on heuristic
inferred from title
author name string
B Stallmeyer
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
H Fenge
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
U Nowak-Göttl
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
E Schulze-Bahr
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
publication date
1 December 2010
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
volume
78
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
page(s)
533-540
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
cites work
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
1 reference
stated in
COCI
retrieved
4 November 2023
reference URL
https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE01827
Identifiers
DOI
10.1111/J.1399-0004.2010.01422.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
PubMed publication ID
20456451
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20456451
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20456451%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
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