Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect-Reference-Cited by-同舟云学术

Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect

Published:2015-12 Issue:1 Volume:8 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Zhang Jingjing,Ma Dingyuan,Wang Yan,Cao Li,Wu Yun,Qiao Fengchang,Liu An,Li Li,Lin Ying,Liu Gang,Liu Cuiyun,Hu Ping,Xu Zhengfeng

Funder

National Natural Science Foundation of China

Jiangsu Natural Science Foundation

Medical Leading Talent and Innovation Team Project of Jiangsu Province

the Key Technology R&D Program of Jiangsu Province

the Foundation of Jiangsu Provincial Department of Health

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-015-0209-5.pdf

Reference28 articles.

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2. Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. 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. Lancet. 2012;380:2095–128.

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

4. Bellucco FT, Belangero SI, Farah LM, Machado MV, Cruz AP, Lopes LM, et al. Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography. Pediatr Cardiol. 2010;31:1146–50.

5. Scambler PJ. The 22q11 deletion syndromes. Hum Mol Genet. 2000;9:2421–6.

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