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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cai, Meiying, Huang, Hailong, Xu, Liangpu, Lin, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Molecular Biosciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167038/
https://www.ncbi.nlm.nih.gov/pubmed/34084776
http://dx.doi.org/10.3389/fmolb.2021.666115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167038/
https://www.ncbi.nlm.nih.gov/pubmed/34084776
http://dx.doi.org/10.3389/fmolb.2021.666115

Ejemplares similares