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The epidemiology and genetics of congenital heart disease
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
The epidemiology and genetics of congenital heart disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
main subject
congenital disorder
0 references
epidemiology
1 reference
based on heuristic
inferred from title
author name string
Goldmuntz E
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
publication date
1 March 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
published in
Clinics in Perinatology
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
volume
28
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
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31 July 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
page(s)
1-10
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
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31 July 2017
cites work
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
1 reference
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Crossref
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7 January 2021
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Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome
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reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations
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reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects
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reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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Familial risks of congenital heart defect assessed in a population-based epidemiologic study.
1 reference
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https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11
1 reference
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https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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Five Instances of Persistent Ductus Arteriosus in One Sibship
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https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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X-linked situs abnormalities result from mutations in ZIC3
1 reference
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7 January 2021
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Frequency of 22q11 deletions in patients with conotruncal defects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Down syndrome phenotypes: the consequences of chromosomal imbalance
1 reference
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Crossref
reference URL
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7 January 2021
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Jagged1 mutations in patients ascertained with isolated congenital heart defects
1 reference
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Crossref
reference URL
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7 January 2021
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Retinoic acid embryopathy
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Congenital heart disease in Down's syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tetralogy of Fallot associated with chromosome 22q11 deletion
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Update on counseling the family with a first-degree relative with a congenital heart defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease caused by mutations in the transcription factor NKX2-5
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
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7 January 2021
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inferred from DOI database lookup
Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 22q11 microdeletions in tetralogy of Fallot
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease in infants with Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0095-5108%2805%2970067-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0095-5108(05)70067-1
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
PubMed ID
11265502
1 reference
stated in
Europe PubMed Central
PubMed ID
11265502
retrieved
31 July 2017
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