Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference26 articles.
1. Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis;Gil;Ultrasound Obstet Gynecol,2015
2. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study;Palomaki;Genet Med,2011
3. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing;Bianchi;Obstet Gynecol,2012
4. 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
5. 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
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1. Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study;Archives of Gynecology and Obstetrics;2024-05-30
2. Ultrasound signs of fetal chromosomal abnormalities at 11–14 weeks of pregnancy and its value in the era of modern genetic testing;Ultrasound & Functional Diagnostics;2024-02-13
3. Low first-trimester fetal fraction is associated with chronic inflammation in the placenta;American Journal of Obstetrics & Gynecology MFM;2023-08
4. Laboratory methods for prenatal diagnosis;Medicine and ecology;2023-07-23
5. Cell-free DNA Screening for Aneuploidy;Clinical Obstetrics & Gynecology;2023-07-17
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