Non‐invasive prenatal diagnosis for Down syndrome: the paradigm will shift, but slowly
Open Access
- 25 January 2012
- journal article
- opinion
- Published by Wiley in Ultrasound in Obstetrics & Gynecology
- Vol. 39 (2) , 127-130
- https://doi.org/10.1002/uog.11083
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011Prenatal Diagnosis, 2012
- Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA SequencingPLOS ONE, 2011
- Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011Prenatal Diagnosis, 2011
- Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical settingAmerican Journal of Obstetrics and Gynecology, 2011
- Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation SequencingScience Translational Medicine, 2011
- Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity studyBMJ, 2011
- Chromosome abnormalities investigated by non‐invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypesAmerican Journal of Medical Genetics Part A, 2010
- Two‐stage first‐trimester screening for trisomy 21 by ultrasound assessment and biochemical testingUltrasound in Obstetrics & Gynecology, 2010
- Fetal Cells and Cell Free Fetal Nucleic Acids in Maternal Blood: New Tools to Study Abnormal Placentation?Placenta, 2005
- The Safety and Efficacy of Chorionic Villus Sampling for Early Prenatal Diagnosis of Cytogenetic AbnormalitiesNew England Journal of Medicine, 1989