(Q80534361)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

Congenital cardiac disease and inbreeding: specific defects escape higher risk due to parental consanguinity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

Ghassan Chehab

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Philippe Chedid

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Zakhia Saliba

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Patrice Bouvagnet

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

27 June 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

published in

Cardiology in the Young

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

414-422

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2).

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Inbreeding and congenital heart diseases in a north Indian population.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Incidence and spectrum of congenital heart disease in Oman

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Parental consanguinity and congenital heart malformations in a developing country.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Birth defects and parental consanguinity in Norway

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Consanguinity and congenital heart disease in the rural Arab population in northern Israel

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

A second-generation study of 427 probands with congenital heart defects and their 837 children

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Congenital heart disease caused by mutations in the transcription factor NKX2-5

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Contribution of birth defects to infant mortality in the United States

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Incidence of congenital heart disease in Qatari children

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Mutation in myosin heavy chain 6 causes atrial septal defect

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Familial atrioventricular septal defect: possible genetic mechanisms

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Consanguinity and complex cardiac anomalies with situs ambiguus

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Mutations in NOTCH1 cause aortic valve disease

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Consanguinity and congenital heart disease in Saudi Arabia

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

NKX2.5 mutations in patients with tetralogy of fallot

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

Risk factors for congenital heart diseases in Alexandria, Egypt

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations

1 reference

https://api.crossref.org/works/10.1017%2FS1047951107000704

7 January 2021

10.1017/S1047951107000704

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594737%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference