Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era

Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era

Abstract In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21.

Bibliographic Details
Main Authors: Evy Vervecken, Bettina Blaumeiser, Tina Vanderheyden, Jan Hauspy, Katrien Janssens
Format: Article
Language:English
Published: Wiley 2020-08-01
Series:Clinical Case Reports
Subjects:
amniocentesis
deletion chromosome 13
holoprosencephaly
invasive prenatal diagnosis
NIPT
noninvasive prenatal test
Online Access:https://doi.org/10.1002/ccr3.2889

Internet

https://doi.org/10.1002/ccr3.2889

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