Validation of an Enhanced Version of a Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies
Author(s) -
Allison Ryan,
Nathan Hunkapiller,
Milena Banjevic,
Naresh Vankayalapati,
Nicole L. Fong,
Kristine N. Jinnett,
Zachary Demko,
Bernhard Zimmermann,
Styrmir Sigurjonsson,
Susan J. Gross,
Matthew D. Hill
Publication year - 2016
Publication title -
fetal diagnosis and therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 60
eISSN - 1421-9964
pISSN - 1015-3837
DOI - 10.1159/000442931
Subject(s) - medicine , prenatal diagnosis , fetus , single nucleotide polymorphism , aneuploidy , obstetrics , nuchal translucency , pregnancy , genetics , genotype , biology , gene , chromosome
To validate an updated version (Version 2) of a single-nucleotide polymorphism (SNP)-based noninvasive prenatal test (NIPT) and to determine the likelihood of success when testing for fetal aneuploidies following a redraw.
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