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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465655/
https://www.ncbi.nlm.nih.gov/pubmed/30767419
http://dx.doi.org/10.1002/mgg3.597

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465655/
https://www.ncbi.nlm.nih.gov/pubmed/30767419
http://dx.doi.org/10.1002/mgg3.597

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