A first look at women's perspectives on noninvasive prenatal testing to detect sex chromosome aneuploidies and microdeletion syndromes
Author:
Affiliation:
1. Department of Bioethics; Cleveland Clinic; Cleveland OH USA
2. Genomic Medicine Institute; Cleveland Clinic; Cleveland OH USA
3. Department of Obstetrics & Gynecology; Cleveland Clinic Women's Health Institute; Cleveland OH USA
Funder
March of Dimes Foundation
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4594/fullpdf
Reference46 articles.
1. Non-invasive prenatal testing using cell free DNA in maternal plasma: recent developments and future prospects;Benn;J Clin Med,2014
2. Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study;Chiu;BMJ,2011
3. DNA sequencing versus standard prenatal aneuploidy screening;Bianchi;N Engl J Med,2014
4. Chromosomal microarray versus haryotyping for prenatal diagnosis;Wapner;N Engl J Med,2012
5. DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study;Palomaki;Genet Med,2012
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