Somatic mutations inNKX2-5,GATA4, andHAND1are not a common cause of tetralogy of Fallot or hypoplastic left heart-Reference-Cited by-同舟云学术

Somatic mutations inNKX2-5,GATA4, andHAND1are not a common cause of tetralogy of Fallot or hypoplastic left heart

Published:2011-08-16 Issue:10 Volume:155 Page:2416-2421
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Esposito Giorgia,Butler Tanya L.,Blue Gillian M.,Cole Andrew D.,Sholler Gary F.,Kirk Edwin P.,Grossfeld Paul,Perryman Benjamin M.,Harvey Richard P.,Winlaw David S.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34187/fullpdf

Reference23 articles.

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3. Recurrence risks in offspring of adults with major heart defects: Results from first cohort of British collaborative study;Burn;Lancet,1998

4. Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE);Dasgupta;Mutat Res,2001

5. Investigation of somatic NKX 2-5 mutations in congenital heart disease;Draus;J Med Genet,2009

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