A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects-Reference-Cited by-同舟云学术

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A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects

Published:2020-07-31 Issue: Volume:7 Page:
ISSN:2297-055X
Container-title:Frontiers in Cardiovascular Medicine
language:
Short-container-title:Front. Cardiovasc. Med.

Author:

Cheng Liangping,Tang Yanlai,Lin Yuese,Ba Hongjun,Ding Yiqian,Chen Dubo,Liu Min,Pan Peizhen,Qin Youzhen,Huang Zhan-Peng

Funder

National Natural Science Foundation of China

Guangdong Science and Technology Department

Fundamental Research Funds for the Central Universities

Publisher

Frontiers Media SA

Subject

Cardiology and Cardiovascular Medicine

Reference25 articles.

1. Genetic testing in congenital heart disease: ethical considerations;Lin;World J Pediatr Congenit Heart Surg.,2013

2. Perinatal and follow- up outcome study of fetal anomalies with multidisciplinary consultation;Li;Ther Clin Risk Manage.,2017

3. Outcome and requirement for surgical repair following prenatal diagnosis of ventricular septal defect;Mosimann;Ultrasound Obstet Gynecol.,2014

4. Chromosomal abnormalities and copy number variations in fetal ventricular septal defects;Cai;Mol Cytogenet.,2018

5. Congenital heart disease and genetic syndromes: new insights into molecular mechanisms;Calcagni;Expert Rev Mol Diagn.,2017

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