Open AccessTerminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era
Author(s) -
Vervecken Evy,
Blaumeiser Bettina,
Vanderheyden Tina,
Hauspy Jan,
Janssens Katrien
Publication year - 2020
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.2889
Subject(s) - medicine , prenatal diagnosis , fetus , obstetrics , chromosome , genetics , pregnancy , biology , gene
In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21.