Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities

BACKGROUND: The current gold standard of karyotype analysis for prenatal diagnosis of fetuses with central nervous system (CNS) abnormalities has some limitations. Here, we assessed the value of single nucleotide polymorphism (SNP) arrays as a diagnostic tool. METHODS: The results of prenatal diagno...

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Detalles Bibliográficos
Autores principales: Xie, Xiaorui, Wu, Xiaoqing, Su, Linjuan, Cai, Meiying, Li, Ying, Huang, Hailong, Xu, Liangpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354765/
https://www.ncbi.nlm.nih.gov/pubmed/34393503
http://dx.doi.org/10.2147/IJGM.S323899

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354765/
https://www.ncbi.nlm.nih.gov/pubmed/34393503
http://dx.doi.org/10.2147/IJGM.S323899

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