Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies

BACKGROUND: Single nucleotide polymorphism array (SNP-array) has been introduced for prenatal diagnosis. We aimed to evaluate the clinical value of SNP-array in the diagnosis of fetal chromosomal anomalies. METHODS: A retrospective study was conducted on 5000 cases tested by SNP-array, and the resul...

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Bibliografiska uppgifter
I publikationen:Front Genet
Huvudupphovsmän: Xiang, Jingjing, Ding, Yang, Song, Xiaoyan, Mao, Jun, Liu, Minjuan, Liu, Yinghua, Huang, Chao, Zhang, Qin, Wang, Ting
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2020
Ämnen:
Genetics
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7677511/
https://ncbi.nlm.nih.gov/pubmed/33240322
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.571219
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