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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Prenat Diagn
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2018
Assuntos:
Original Articles
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares