Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array-Reference-Cited by-同舟云学术

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Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array

Published:2018-09-20 Issue:7 Volume:33 Page:1211-1217
ISSN:1476-7058
Container-title:The Journal of Maternal-Fetal & Neonatal Medicine
language:en
Short-container-title:The Journal of Maternal-Fetal & Neonatal Medicine

Author:

Lin Meifang¹,Zheng Ju¹,Peng Ruan¹^ORCID,Du Liu¹,Zheng Qiao¹,Lei Ting¹,Xie Hongning¹

Affiliation:

1. Department of Ultrasonic Medicine and Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China

Funder

National Scientific Foundation Committee of China

Guangdong Provincial Department of Science and Technology

Guangdong Provincial Medical Research Foundation

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/14767058.2018.1517316

Reference28 articles.

1. Prevalence of Congenital Heart Defects in Metropolitan Atlanta, 1998-2005

2. CONGENITAL HEART DISEASE: PREVALENCE AT LIVEBIRTH

3. Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The evolving genetic etiology of conotruncal anomalies;Prenatal Diagnosis;2024-02-16

2. Characteristics of fetal conotruncal heart anomalies;Gulhane Medical Journal;2022-09-07

3. Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-Analysis;Diagnostics;2022-05-27

4. Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis;Diagnostics;2022-02-23

5. Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study;Orphanet Journal of Rare Diseases;2022-01-04

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