The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis

Background: An increase in pathogenic copy number variants (pCNVs) has been recognized to associate with fetal growth restriction (FGR). Here, we aim to explore the application value of chromosomal microarray analysis (CMA) in prenatal diagnosis of FGR.Methods: Prenatal ultrasound was applied to ide...

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Detaylı Bibliyografya
Asıl Yazarlar:	Yu'e Chen, Yingjun Xie, Yuying Jiang, Qi Luo, Lijing Shi, Shuhong Zeng, Jianlong Zhuang, Guorong Lyu
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	Frontiers Media S.A. 2021-10-01
Seri Bilgileri:	Frontiers in Pediatrics
Konular:	fetal growth restriction chromosomal microarray analysis karyotype analysis prenatal diagnosis copy number variants (CNVs)
Online Erişim:	https://www.frontiersin.org/articles/10.3389/fped.2021.743639/full
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The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis

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