#36: Prenatal aneuploidy screening using cell-free DNA
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference45 articles.
1. Non-invasive chromosomal evaluation (NICE) study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18;Norton;Am J Obstet Gynecol,2012
2. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study;Palomaki;Genet Med,2011
3. On behalf of the maternal blood is source to accurately diagnose fetal aneuploidy (MELISSA) study group: genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing;Bianchi;Obstet Gynecol,2012
4. Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18;Sparks;Am J Obstet Gynecol,2012
5. Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci;Zimmermann;Prenat Diagn,2012
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2. First‐ and Second‐Trimester Screening for Fetal Aneuploidy and Neural Tube Defects;Queenan's Management of High‐Risk Pregnancy;2023-12
3. Genetic counseling practices among outpatient obstetric providers in the Northeast;American Journal of Obstetrics & Gynecology MFM;2023-11
4. How to choose a test for prenatal genetic diagnosis: a practical overview;American Journal of Obstetrics and Gynecology;2023-02
5. Implications for Prenatal Genetic Testing in the United States After the Reversal of Roe v Wade;Obstetrics & Gynecology;2023-01-18
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