Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT

BACKGROUND: Non‐invasive prenatal testing (NIPT) is extensively used in the detection of fetal trisomies 21, 18, and 13, which is promptly becoming a common clinical practice. Concerned about the clinical application of non‐invasive detection of the fetal autosomal duplications or deletion. CASE PRE...

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Detalles Bibliográficos
Autores principales: Zheng, Yunyun, Chen, Biliang, Wan, Shanning, Xu, Hui, Dang, Yinghui, Song, Tingting, Li, Yu, Zhang, Jianfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6818560/
https://www.ncbi.nlm.nih.gov/pubmed/30666717
http://dx.doi.org/10.1002/jcla.22711

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6818560/
https://www.ncbi.nlm.nih.gov/pubmed/30666717
http://dx.doi.org/10.1002/jcla.22711

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