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 2011
- 24 January 2012
- journal article
- practice guideline
- Published by Wiley in Prenatal Diagnosis
- Vol. 32 (1) , 1-2
- https://doi.org/10.1002/pd.2919
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Optimal Detection of Fetal Chromosomal Abnormalities by Massively Parallel DNA Sequencing of Cell-Free Fetal DNA from Maternal BloodClinical Chemistry, 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
- Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity studyBMJ, 2011