Does the risk for high-penetrant copy number variants in low-risk pregnancies exceed the risk of miscarriage after invasive testing?-Reference-Cited by-同舟云学术

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Does the risk for high-penetrant copy number variants in low-risk pregnancies exceed the risk of miscarriage after invasive testing?

Published:2023-11 Issue: Volume: Page:101232
ISSN:2589-9333
Container-title:American Journal of Obstetrics & Gynecology MFM
language:en
Short-container-title:American Journal of Obstetrics & Gynecology MFM

Author:

Yang Yan-Dong,Li Dong-Zhi

Publisher

Elsevier BV

Subject

General Medicine,Obstetrics and Gynecology

Reference4 articles.

1. Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies;Sagi-Dain;Genet Med,2019

2. Is it time for prenatal chromosomal-microarray analysis to all women? A review of the diagnostic yield in structurally normal fetuses;Daum;Curr Opin Obstet Gynecol,2021

3. Prevalence of high-penetrant copy number variants in 7,734 low-risk pregnancies;Sagi-Dain;Am J Obstet Gynecol MFM,2023

4. Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy-number variants;Soster;Genet Med,2021

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