Committee Opinion No. 640
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Obstetrics and Gynecology
Reference24 articles.
1. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing. MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Grouppublished erratum appears in Obstet Gynecol 2012;120:957.;Bianchi;Obstet Gynecol,2012
2. . Presence of fetal DNA in maternal plasma and serum.;Lo;Lancet,1997
3. Rapid clearance of fetal DNA from maternal plasma.;Lo;Am J Hum Genet,1999
4. . DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.;Palomaki;Genet Med,2011
5. . Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.;Sparks;Prenat Diagn,2012
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1. Prenatal cell-free DNA screening for chromosomal aneuploidies after euploid embryo transfer shows high concordance with preimplantation genetic testing for aneuploidy results and low positive predictive values;Fertility and Sterility;2024-07
2. Selection of prenatal screening with nuchal translucency > 95th centile and below 99th centile: a 4-year observational study with real-world data;Archives of Gynecology and Obstetrics;2024-04-16
3. Performance of cell‐free DNA testing for common fetal trisomies in triplet pregnancies;Prenatal Diagnosis;2024-03-06
4. Residual risk of clinically significant copy number variations in fetuses with nasal bone absence or hypoplasia after excluding non-invasive prenatal screening-detectable findings;Clinica Chimica Acta;2024-01
5. The Dysmorphic Infant;Avery's Diseases of the Newborn;2024
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