Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies

Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies

The association between genetics and fetuses with ventriculomegaly (VM) is unknown. This study aimed to classify and evaluate abnormal copy number variations (CNVs) in fetuses with VM. From December 2016 to September 2020, amniotic fluid or umbilical cord blood from 293 pregnant women carrying fetus...

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Bibliographic Details
Main Authors: Meiying Cai, Hailong Huang, Liangpu Xu, Na Lin
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Genetics
Subjects:
ventriculomegaly
copy number variation
SNP-array
fetal screening
genetic evaluation
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.682707/full

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2021.682707/full

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