Correlation between types of ventricular septal defect and chromosomal abnormalities in low-risk non-invasive prenatal testing-Reference-Cited by-同舟云学术

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Correlation between types of ventricular septal defect and chromosomal abnormalities in low-risk non-invasive prenatal testing

Published:2024-06-26 Issue:3 Volume:310 Page:1517-1523
ISSN:1432-0711
Container-title:Archives of Gynecology and Obstetrics
language:en
Short-container-title:Arch Gynecol Obstet

Author:

Zhao Xiaomin,Shen Yongmei,Kong Dexuan,Li Wen,Yao Liying,Li Shanshan,Chang Ying^ORCID

Funder

National Key Specialties and Diseases Cohort Project

Natural Science Foundation of Tianjin

pen Fund of Tianjin Central Hospital of Gynecology Obstetrics/Tianjin Key Laboratory of human development and reproductive regulation

Open Fund of Tianjin Central Hospital of Gynecology Obstetrics/Tianjin Key Laboratory of human development and reproductive regulation

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s00404-024-07566-3.pdf

Reference15 articles.

1. Eckerström F, Nyboe C, Maagaard M et al (2023) Survival of patients with congenital ventricular septal defect. Eur Heart J 44:54–61. https://doi.org/10.1093/eurheartj/ehac618

2. Cheng K, Zhou H, Fu F et al (2022) Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China. Front Cardiovasc Med 9:988438. https://doi.org/10.3389/fcvm.2022.988438

3. RaucherSternfeld A, Sheffy A, Tamir A et al (2022) Isolated ventricular septal defects demonstrated by fetal echocardiography: prenatal course and postnatal outcome. J Matern Fetal Neonatal 35:129–133. https://doi.org/10.1080/14767058.2020.1712710

4. Chen Y, Lu L, Zhang Y et al (2022) Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnancies. Am J Med Genet A 188:1426–1434. https://doi.org/10.1002/ajmg.a.62657

5. Yu D, Zhang K, Han M et al (2019) Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing. Mol Genet Genomic Med 7:e674. https://doi.org/10.1002/mgg3.674

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