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English
Isolation of the subclavian artery associated with chromosome 22q11 deletion
scientific article published on 01 March 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
title
Isolation of the subclavian artery associated with chromosome 22q11 deletion
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
K Momma
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 March 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Cardiology in the Young
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
233-235
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
Truncus arteriosus communis associated with chromosome 22q11 deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tetralogy of Fallot associated with chromosome 22q11 deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rare forms of isolation of the subclavian artery: echocardiographic diagnosis and surgical considerations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac neural crest is essential for the persistence rather than the formation of an arch artery
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fetal cardiovascular morphology of truncus arteriosus with or without truncal valve insufficiency in the rat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of neural crest in congenital heart disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neural crest and cardiovascular patterning.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of 22q11 deletions in patients with conotruncal defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1047951100008532
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S1047951100008532
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed publication ID
10323529
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10323529
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10323529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
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