Copy number variations in the GATA4 , NKX2-5 , TBX5 , BMP4 CRELD1 , and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease-Reference-Cited by-同舟云学术

Copy number variations in the GATA4 , NKX2-5 , TBX5 , BMP4 CRELD1 , and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease

Published:2018-09-17 Issue:2 Volume:33 Page:e22660
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Li Zhetao¹^ORCID,Huang Jiwei¹,Liang Biao²,Zeng Dingyuan³,Luo Shiqiang¹,Yan Tizhen¹,Liao Fengwen²,Huang Jun¹,Li Jingwen¹,Cai Ren¹,Deng Xine⁴,Tang Ning¹

Affiliation:

1. Department of Medical Genetics; Liuzhou Maternal and Children Healthcare Hospital; Liuzhou China

2. Department of Pediatrics Surgery; Liuzhou Maternal and Children Healthcare Hospital; Liuzhou China

3. Deparment of Gynaecology and Obstetrics; Liuzhou Maternal and Children Healthcare Hospital; Liuzhou China

4. Department of the Perinatal Division; Liuzhou Maternal and Children Healthcare Hospital; Liuzhou China

Funder

Guangxi Scientific Research Technology Development Project

Liuzhou Science and Technology Development Program

Guangxi Zhuang Region Health Department

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcla.22660/fullpdf

Reference23 articles.

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2. Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics;Pierpont;Circulation,2007

3. 22q11.2 deletion syndrome in diverse populations;Kruszka;Am J Med Genet A,2017

4. Increased frequency of de novo copy number variations in congenital heart disease by integrative analysis of SNP-array and exome sequence data;Glessner;Circ Res,2014

5. Advances in the understanding of the genetic determinants of congenital heart disease and their impact on clinical outcomes;Russell;J Am Heart Assoc,2018

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