Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y
Author:
Affiliation:
1. Harris Birthright Research Centre for Fetal Medicine; King's College Hospital; London UK
2. Department of Fetal Medicine; University College London Hospital; London UK
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4103/fullpdf
Reference25 articles.
1. Screening for fetal aneuploidies at 11 to 13 weeks;Nicolaides;Prenat Diagn,2011
2. Presence of fetal DNA in maternal plasma and serum;Lo;Lancet,1997
3. Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study;Chiu;BMJ,2011
4. Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting;Ehrich;Am J Obstet Gynecol,2011
5. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study;Palomaki;Genet Med,2011
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