Comprehensive non-invasive prenatal screening for pregnancies with elevated risks of genetic disorders: protocol for a prospective, multicentre study

INTRODUCTION: Chromosomal abnormalities and monogenic disorders account for ~15%–25% of recognisable birth defects. With limited treatment options, preconception and prenatal screening were developed to reduce the incidence of such disorders. Currently, non-invasive prenatal screening (NIPS) for com...

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Detalles Bibliográficos
Autores principales: Xu, Chenming, Cai, Xiaoqiang, Chen, Songchang, Luo, Qiong, Xi, Hui, Zhang, Dan, Wang, Hua, Wu, Yanting, Huang, He-Feng, Zhang, Jinglan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Diagnostics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404451/
https://www.ncbi.nlm.nih.gov/pubmed/34452972
http://dx.doi.org/10.1136/bmjopen-2021-053617

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404451/
https://www.ncbi.nlm.nih.gov/pubmed/34452972
http://dx.doi.org/10.1136/bmjopen-2021-053617

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