Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population-Reference-Cited by-同舟云学术

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Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

Published:2015-12 Issue:1 Volume:9 Page:
ISSN:1755-8794
Container-title:BMC Medical Genomics
language:en
Short-container-title:BMC Med Genomics

Author:

An Yu,Duan Wenyuan,Huang Guoying,Chen Xiaoli,Li Li,Nie Chenxia,Hou Jia,Gui Yonghao,Wu Yiming,Zhang Feng,Shen Yiping,Wu Bailin,Wang Hongyan

Funder

973 National Basic Research Program of China

the National Natural Science Foundation of China

Ministry of Education of the People's Republic of China (CN)

the Commission for Science and Technology of Shanghai Municipality

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12920-015-0163-4

Reference36 articles.

1. Hoffman JI, Kaplan S. The incidence of congenital heart disease. J Am Coll Cardiol. 2002;39(12):1890–900.

2. Gruber PJ, Epstein JA. Development gone awry: congenital heart disease. Circ Res. 2004;94(3):273–83.

3. Otterstad JE, Nitter-Hauge S, Myhre E. Isolated ventricular septal defect in adults. Clinical and haemodynamic findings. Br Heart J. 1983;50(4):343–8.

4. Hartman RJ, Rasmussen SA, Botto LD, Riehle-Colarusso T, Martin CL, Cragan JD, et al. The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study. Pediatr Cardiol. 2011;32(8):1147–57.

5. Breckpot J, Thienpont B, Peeters H, de Ravel T, Singer A, Rayyan M, et al. Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects. J Pediatr. 2010;156(5):810–7. 817 e811-817 e814.

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