Evaluation of non‐invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort

The aim of this study was to evaluate the clinical feasibility of non‐invasive prenatal testing (NIPT) to detect foetal copy number variations (CNVs). Next‐generation sequencing for detecting foetal copy number variations (CNVs) was performed on the collected samples from 161 pregnancies with ultras...

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Detalles Bibliográficos
Autores principales: Cui, Wanting, Liu, Xiaoliang, Zhang, Yuanyuan, Wang, Yueping, Chu, Guoming, He, Rong, Zhao, Yanyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Short Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815821/
https://www.ncbi.nlm.nih.gov/pubmed/31454164
http://dx.doi.org/10.1111/jcmm.14614

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815821/
https://www.ncbi.nlm.nih.gov/pubmed/31454164
http://dx.doi.org/10.1111/jcmm.14614

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