Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference38 articles.
1. Noninvasive prenatal testing: the paradigm is shifting rapidly;Chitty;Prenat Diagn,2013
2. Single-nucleotide polymorphism-based noninvasive prenatal testing in a high-risk and low-risk cohort;Pergament;Obstet Gynecol,2014
3. Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y;Nicolaides;Prenat Diagn,2013
4. SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy;Samango-Sprouse;Prenat Diagn,2013
5. Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood;Nicolaides;Fetal Diagn Ther,2014
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1. Cell‐free DNA test for fetal chromosomal abnormalities in multiple pregnancies;Acta Obstetricia et Gynecologica Scandinavica;2024-06-25
2. Test performance and clinical utility of expanded non‐invasive prenatal test: Experience on 71,883 unselected routine cases from one single center;Prenatal Diagnosis;2024-04-30
3. High positive predictive value 22q11.2 microdeletion screening by prenatal cell‐free DNA testing that incorporates fetal fraction amplification;Prenatal Diagnosis;2024-04-15
4. A statistical investigation of parameters associated with low cell-free fetal DNA fraction in maternal plasma for noninvasive prenatal testing;The Journal of Maternal-Fetal & Neonatal Medicine;2024-01-02
5. Noninvasive prenatal screening for fetal aneuploidies;Diagnostic Molecular Pathology;2024
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