(Q44724940)

5 December 2017

title

Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle (English)

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5 December 2017

Z-P Tan

1

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5 December 2017

C Huang

2

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5 December 2017

Z-B Xu

3

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5 December 2017

J-F Yang

4

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5 December 2017

Y-F Yang

5

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5 December 2017

publication date

30 October 2011

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5 December 2017

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5 December 2017

volume

82

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5 December 2017

issue

5

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5 December 2017

page(s)

466-471

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The incidence of congenital heart disease

5 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Congenital Heart Surgery Nomenclature and Database Project: double outlet right ventricle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Double outlet right ventricle: aetiologies and associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Disruption of friend of GATA 2 gene (FOG-2) by a de novo t(8;10) chromosomal translocation is associated with heart defects and gonadal dysgenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Molecular cloning of FOG-2: a modulator of transcription factor GATA-4 in cardiomyocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Fog2 is required for normal diaphragm and lung development in mice and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Towards a structural basis of human non-synonymous single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

MutationTaster evaluates disease-causing potential of sequence alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Fibrous skeleton and ventricular outflow tracts in double-outlet right ventricle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Biventricular repair in double outlet right ventricle: surgical results based on the STS-EACTS International Nomenclature classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01787.X

10.1111/J.1399-0004.2011.01787.X

21 January 2018

Identifiers

DOI

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5 December 2017

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