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English
Getting to the heart of DiGeorge syndrome
scientific article published on 01 October 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Getting to the heart of DiGeorge syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
main subject
DiGeorge syndrome
1 reference
based on heuristic
inferred from title
author name string
Schinke M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Izumo S
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 October 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Nature Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
1120-1121
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/13438
0 references
cites work
A common molecular basis for rearrangement disorders on chromosome 22q11
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease in mice deficient for the DiGeorge syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
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/10.1038%2F13438
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/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13438
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/13438
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
10502806
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10502806
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10502806%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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