(Q47644393)

English

Patterns of recurrence of congenital heart disease: an analysis of 6,640 consecutive pregnancies evaluated by detailed fetal echocardiography

scientific article published in September 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

Patterns of recurrence of congenital heart disease: an analysis of 6,640 consecutive pregnancies evaluated by detailed fetal echocardiography (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

echocardiography

1 reference

based on heuristic

inferred from title

congenital heart disease

1 reference

based on heuristic

inferred from title

author name string

Harinder K Gill

1

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

Miranda Splitt

2

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

Gurleen K Sharland

3

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

John M Simpson

4

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

language of work or name

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publication date

1 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

Journal of the American College of Cardiology

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Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

42

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

5

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

923-929

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

Fetal echocardiography as a predictor of chromosomal abnormality

1 reference

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The evolution of specific genetic and environmental counseling in congenital heart diseases

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7 January 2021

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Pregnancy and its outcome in women with and without surgical treatment of congenital heart disease

1 reference

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7 January 2021

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Familial recurrence of congenital heart disease in a prospective series of mothers referred for fetal echocardiography

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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Nomenclature and classification of congenital heart disease

1 reference

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7 January 2021

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

1 reference

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Assessing familial aggregation of congenital cardiovascular malformations in case-control studies.

1 reference

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Coarctation of the aorta, interrupted aortic arch, and hypoplastic left heart syndrome in three generations

1 reference

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Evidence of congenital heart disease in the offspring of parents with atrioventricular defects

1 reference

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7 January 2021

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

1 reference

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7 January 2021

based on heuristic

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Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canal

1 reference

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7 January 2021

based on heuristic

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

1 reference

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7 January 2021

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Familial congenital valvar pulmonary stenosis: autosomal dominant inheritance

1 reference

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Jagged1 mutations in patients ascertained with isolated congenital heart defects

1 reference

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based on heuristic

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Heterotaxia syndrome and autosomal dominant inheritance.

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Familial situs inversus and congenital heart defects.

1 reference

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X-linked situs abnormalities result from mutations in ZIC3

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Genetics of human situs abnormalities

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Maternal diabetes and cardiovascular malformations: predominance of double outlet right ventricle and truncus arteriosus

1 reference

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7 January 2021

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Familial congenital heart disease: how are the various types related?

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900853-2

7 January 2021

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Concordance and discordance of congenital heart disease in 20 families

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900853-2

7 January 2021

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inferred from DOI database lookup

Heart development: learning from mistakes

1 reference

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7 January 2021

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inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900853-2

7 January 2021

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NKX2.5 mutations in patients with tetralogy of fallot

1 reference

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7 January 2021

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Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

1 reference

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7 January 2021

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Consanguinity and complex cardiac anomalies with situs ambiguus

1 reference

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7 January 2021

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Gene-dosage-sensitive genetic interactions between inversus viscerum (iv), nodal, and activin type IIB receptor (ActRIIB) genes in asymmetrical patterning of the visceral organs along the left-right axis

1 reference

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Identifiers

10.1016/S0735-1097(03)00853-2

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/12957444

ResearchGate publication ID

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