Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y
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Title
Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y
Authors
Keywords
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Journal
PRENATAL DIAGNOSIS
Volume 33, Issue 6, Pages 575-579
Publisher
Wiley
Online
2013-04-24
DOI
10.1002/pd.4103
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- (2012) G. Ashoor et al. ULTRASOUND IN OBSTETRICS & GYNECOLOGY
- Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting
- (2011) Mathias Ehrich et al. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
- Optimal Detection of Fetal Chromosomal Abnormalities by Massively Parallel DNA Sequencing of Cell-Free Fetal DNA from Maternal Blood
- (2011) A. J. Sehnert et al. CLINICAL CHEMISTRY
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- (2008) R. W. K. Chiu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood
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- A mixture model of nuchal translucency thickness in screening for chromosomal defects
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