Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population
Author:
Affiliation:
1. Obstetrics and Gynecology of Atlanta; Atlanta GA USA
2. Ariosa Diagnostics; San Jose CA USA
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4092/fullpdf
Reference17 articles.
1. Noninvasive 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. Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population;Nicolaides;Am J Obstet Gynecol,2012
3. Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18;Ashoor;Am J 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. Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy;Sparks;Prenat Diagn,2012
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