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 id...

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Detalles Bibliográficos
Autores principales: Chen, Yu'e, Xie, Yingjun, Jiang, Yuying, Luo, Qi, Shi, Lijing, Zeng, Shuhong, Zhuang, Jianlong, Lyu, Guorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555260/
https://www.ncbi.nlm.nih.gov/pubmed/34722424
http://dx.doi.org/10.3389/fped.2021.743639

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555260/
https://www.ncbi.nlm.nih.gov/pubmed/34722424
http://dx.doi.org/10.3389/fped.2021.743639

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