Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities

Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities

Applying single nucleotide polymorphism (SNP) array to identify the etiology of fetal central nervous system (CNS) abnormality, and exploring its association with chromosomal abnormalities, copy number variations, and obstetrical outcome. 535 fetuses with CNS abnormalities were analyzed using karyot...

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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. 2021-05-01
Series:Frontiers in Molecular Biosciences
Subjects:
central nervous system
copy number variations
obstetrics
SNP-array
prenatal assessment
Online Access:https://www.frontiersin.org/articles/10.3389/fmolb.2021.666115/full

Internet

https://www.frontiersin.org/articles/10.3389/fmolb.2021.666115/full

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