Whole Exome Sequencing Identifies A Novel Pathogenic Bmpr2 Variant in Pulmonary Atresia-Reference-Cited by-同舟云学术

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Whole Exome Sequencing Identifies A Novel Pathogenic Bmpr2 Variant in Pulmonary Atresia

Published:2021 Issue:5 Volume:16 Page:487-498
ISSN:1747-079X
Container-title:Congenital Heart Disease
language:en
Short-container-title:

Author:

Qi Muyu,Lan Xiaoping,Li Jia,Ge Junwen,Shen Li,Zhang Rufang

Publisher

Computers, Materials and Continua (Tech Science Press)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine,Surgery,Pediatrics, Perinatology and Child Health

Reference38 articles.

1. Advances in molecular genetics for pulmonary atresia;Gao;Cardiology in the Young,2017

2. Long-term outcomes of single-ventricle palliation for pulmonary atresia with intact ventricular septum: Fontan survivors remain at risk of late myocardial ischaemia and death;Elias;European Journal of Cardio-Thoracic Surgery: Official Journal of the European Association for Cardio-thoracic Surgery,2018

3. Prenatal diagnosis of pulmonary atresia with ventricular septal defect;Yang;Journal of Medical Ultrasonics,2018

4. Rare de novo copy number variants in patients with congenital pulmonary atresia;Xie;PLoS One,2014

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