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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3. First‐ and Second‐Trimester Screening for Fetal Aneuploidy and Neural Tube Defects;Queenan's Management of High‐Risk Pregnancy;2023-12
4. Comparison of web-based information about cell-free DNA prenatal screening: implications for differences of sex development care;Frontiers in Urology;2023-10-31
5. Non-Invasive Prenatal Testing (NIPT) for Aneuploidy in a Setting with a High Consanguineous Rate – A Retrospective Cohort Review of 1,153 Cases;Qeios;2023-09-04
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