(Q37760244)

22 August 2017

1 reference

title

Genetic factors in non-syndromic congenital heart malformations (English)

1 reference

22 August 2017

0 references

M W Wessels

1

1 reference

PubMed ID

20497191

22 August 2017

P J Willems

series ordinal

2

1 reference

22 August 2017

17 May 2010

1 reference

22 August 2017

1 reference

22 August 2017

78

1 reference

22 August 2017

2

1 reference

22 August 2017

103-123

1 reference

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

22 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

In vivo modeling of myosin binding protein C familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Failure to detect connexin43 mutations in 38 cases of sporadic and familial heterotaxy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Heart defects in connexin43-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Dohi Memorial Lecture. New aspects of cutaneous mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01435.X

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

21 January 2018

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE01827

Mutations in NOTCH1 cause aortic valve disease

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE03940

Identifiers

DOI

10.1111/J.1399-0004.2010.01435.X

1 reference

22 August 2017

1 reference

PubMed ID

20497191