Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis
Top Cited Papers
- 24 April 2013
- journal article
- practice guideline
- Published by Wiley in Prenatal Diagnosis
- Vol. 33 (7) , 622-629
- https://doi.org/10.1002/pd.4139
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Chromosomal Microarray versus Karyotyping for Prenatal DiagnosisNew England Journal of Medicine, 2012
- The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomyThe Journal of Maternal-Fetal & Neonatal Medicine, 2012
- Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA SequencingObstetrics & Gynecology, 2012
- DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative studyGenetics in Medicine, 2012
- 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
- A reassessment of biochemical marker distributions in trisomy 21‐affected and unaffected twin pregnancies in the first trimesterUltrasound in Obstetrics & Gynecology, 2010
- First trimester aneuploidy screening in the presence of a vanishing twin: implications for maternal serum markersPrenatal Diagnosis, 2010
- Role of Second-Trimester Genetic Sonography After Down Syndrome ScreeningObstetrics & Gynecology, 2009
- Likelihood ratio for trisomy 21 in fetuses with absent nasal bone at the 11–14‐week scanUltrasound in Obstetrics & Gynecology, 2004