Reliable detection of subchromosomal deletions and duplications using cell‐based noninvasive prenatal testing

OBJECTIVE: To gather additional data on the ability to detect subchromosomal abnormalities of various sizes in single fetal cells isolated from maternal blood, using low‐coverage shotgun next‐generation sequencing for cell‐based noninvasive prenatal testing (NIPT). METHOD: Fetal trophoblasts were re...

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Vydáno v:Prenat Diagn
Hlavní autoři: Vossaert, Liesbeth, Wang, Qun, Salman, Roseen, Zhuo, Xinming, Qu, Chunjing, Henke, David, Seubert, Ron, Chow, Jennifer, U'ren, Lance, Enright, Brennan, Stilwell, Jackie, Kaldjian, Eric, Yang, Yaping, Shaw, Chad, Levy, Brynn, Wapner, Ronald, Breman, Amy, Van den Veyver, Ignatia, Beaudet, Arthur
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2018
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6587831/
https://ncbi.nlm.nih.gov/pubmed/30357877
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.5377
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