Applying high‐throughput sequencing to identify and evaluate foetal chromosomal deletion and duplication

The present study aimed to estimate the clinical performance of non‐invasive prenatal testing (NIPT) based on high‐throughput sequencing method for the detection of foetal chromosomal deletions and duplications. A total of 6348 pregnant women receiving NIPT using high‐throughput sequencing method we...

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Detalles Bibliográficos
Autores principales: Wu, Yueli, Zhang, Linlin, Lv, Hong, Li, Ying, Zhu, Chongyang, Tian, Weifang, Zhao, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520324/
https://www.ncbi.nlm.nih.gov/pubmed/32667743
http://dx.doi.org/10.1111/jcmm.15593

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520324/
https://www.ncbi.nlm.nih.gov/pubmed/32667743
http://dx.doi.org/10.1111/jcmm.15593

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