Pilot study of a novel multi‐functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single‐gene disorder screening

BACKGROUND: The noninvasive prenatal testing (NIPT) has been successfully used in the clinical screening of fetal trisomy 13, 18, and 21 in the last few years and researches on detecting sub‐chromosomal copy number variations (CNVs) and monogenic diseases are also in progress. To date, multiple test...

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Bibliografiska uppgifter
I publikationen:Mol Genet Genomic Med
Huvudupphovsmän: Luo, Yuqin, Jia, Bei, Yan, Kai, Liu, Siping, Song, Xiaojie, Chen, Mingfa, Jin, Fan, Du, Yang, Wang, Juan, Hong, Yan, Cao, Sha, Li, Dawei, Dong, Minyue
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2019
Ämnen:
Original Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6465655/
https://ncbi.nlm.nih.gov/pubmed/30767419
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.597
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