Noninvasive prenatal testing for aneuploidy–ready for prime time?
- 1 April 2012
- journal article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 206 (4) , 269-275
- https://doi.org/10.1016/j.ajog.2012.02.021
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Selective analysis of cell‐free DNA in maternal blood for evaluation of fetal trisomyPrenatal Diagnosis, 2012
- Noninvasive prenatal diagnosis: pregnant women's interest and expected uptakePrenatal Diagnosis, 2011
- Cell‐free fetal DNA testing: a pilot study of obstetric healthcare provider attitudes toward clinical implementationPrenatal Diagnosis, 2011
- Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA SequencingPLOS ONE, 2011
- Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity studyBMJ, 2011
- Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide PolymorphismsPLOS ONE, 2010
- Non-invasive prenatal testing: ethical issues exploredEuropean Journal of Human Genetics, 2009
- Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasmaProceedings of the National Academy of Sciences, 2008
- Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal bloodProceedings of the National Academy of Sciences, 2008
- Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detectionNature Medicine, 2007