(Q45899215)

17 December 2017

title

Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallot. (English)

1 reference

17 December 2017

1 reference

Yuan Yuan

1

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17 December 2017

Yan Gao

2

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17 December 2017

Huijun Wang

3

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17 December 2017

Xiaojing Ma

4

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17 December 2017

Duan Ma

5

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17 December 2017

Guoying Huang

6

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17 December 2017

publication date

8 September 2014

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17 December 2017

Birth Defects Research Part A: Clinical and Molecular Teratology

published in

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17 December 2017

volume

100

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17 December 2017

issue

12

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17 December 2017

page(s)

973-984

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17 December 2017

DNA methylation patterns and epigenetic memory

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21 January 2018

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Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

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21 January 2018

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Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening

21 January 2018

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Mutation Analysis of the Vangl2 Coding Region Revealed No Common Cause for Tetralogy of Fallot

21 January 2018

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VANGL2 mutations in human cranial neural-tube defects

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/BDRA.23291

1 reference

17 December 2017

PubMed ID

25200836

1 reference

17 December 2017