The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies
Author:
Affiliation:
1. Division of Medical Screening and Special Testing, Department of Pathology and Laboratory Medicine; Women & Infants Hospital and Alpert Medical School of Brown University; Providence RI 02903 USA
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4126/fullpdf
Reference18 articles.
1. Presence of fetal DNA in maternal plasma and serum;Lo;Lancet,1997
2. Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis;Lo;Am J Hum Genet,1998
3. DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study;Palomaki;Genet Med,2011
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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