Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications-Reference-Cited by-同舟云学术

Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications

Published:2022-08-02 Issue:5 Volume:102 Page:391-403
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

He Guo‐Wei¹²^ORCID,Maslen Cheryl L.³,Chen Huan‐Xin¹,Hou Hai‐Tao¹,Bai Xiao‐Yan¹,Wang Xiu‐Li¹,Liu Xiao‐Cheng¹,Lu Wan‐Li¹,Chen Xin‐Xin⁴,Chen Wei‐Dan⁴,Xing Quan‐Sheng⁵,Wu Qin⁵,Wang Jun¹,Yang Qin¹

Affiliation:

1. Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital Tianjin University & Chinese Academy of Medical Sciences Tianjin China

2. Department of Surgery Oregon Health and Science University Portland Oregon USA

3. Knight Cardiovascular Institute Oregon Health & Science University Portland Oregon USA

4. Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

5. Qingdao Women and Children's Hospital Qingdao University Qingdao China

Funder

Chinese Academy of Medical Sciences

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14201

Reference45 articles.

1. CONGENITAL HEART DISEASE: PREVALENCE AT LIVEBIRTH

2. Trends in congenital anomalies in Europe from 1980 to 2012

3. The current strategy of repair of tetralogy of Fallot in children and adults

4. Low Risk of Pulmonary Valve Implantation After a Policy of Transatrial Repair of Tetralogy of Fallot Delayed Beyond the Neonatal Period

5. Observed Prevalence of Congenital Heart Defects From a Surveillance Study in China

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