Replication of the 4p16 Susceptibility Locus in Congenital Heart Disease in Han Chinese Populations-Reference-Cited by-同舟云学术

Replication of the 4p16 Susceptibility Locus in Congenital Heart Disease in Han Chinese Populations

Published:2014-09-12 Issue:9 Volume:9 Page:e107411
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Zhao Bijun,Lin Yuan,Xu Jing,Ni Bixian,Da Min,Ding Chenyue,Hu Yuanli,Zhang Kai,Yang Shiwei,Wang Xiaowei,Yu Shiqiang,Chen Yijiang,Mo Xuming,Liu Jiayin,Shen Hongbing,Sha Jiahao,Ma Hongxia

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference25 articles.

1. The developmental genetics of congenital heart disease;BG Bruneau;Nature,2008

2. Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis;D van der Linde;J Am Coll Cardiol,2011

3. Prevalence of congenital heart defects in metropolitan Atlanta, 1998–2005;MD Reller;J Pediatr,2008

4. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010;R Lozano;Lancet,2013

5. Hu Z, Yuan X, Rao K, Zheng Z, Hu S (2014) National trend in congenital heart disease mortality in China during 2003 to 2010: A population-based study. J Thorac Cardiovasc Surg 148: 596–602 e591.

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