Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.
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Diagnostic Accuracy of Noninvasive Detection of Fetal Trisomy 21 in Maternal Blood: A Systematic ReviewNoninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012First trimester serum tests for Down's syndrome screeningNon-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issuesNew advances of preimplantation and prenatal genetic screening and noninvasive testing as a potential predictor of health status of babiesNon-invasive prenatal diagnosis of fetal trisomy 21 using cell-free fetal DNA in maternal bloodNon-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsFree DNA--new potential analyte in clinical laboratory diagnostics?Tracking fetal development through molecular analysis of maternal biofluidsIdentification of trisomy 18, trisomy 13, and Down syndrome from maternal plasmaNoninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementRecent advances in prenatal genetic screening and testingAccuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysisDetection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysisIncorporating DNA sequencing into current prenatal screening practice for Down's syndromeMaternal plasma and amniotic fluid sphingolipids profiling in fetal Down syndromeWomen's knowledge, attitudes, and beliefs about Down syndrome: a qualitative research study'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health careNoninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNANoninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencingImplementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yieldCurrent principles and practice of ethics and law in perinatal medicine.Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.Limitations of Aneuploidy and Anomaly Detection in the Obese Patient.DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessmentsEfficient digest of high-throughput sequencing data in a reproducible report.Maternal plasma sequencing: a powerful tool towards fetal whole genome recovery.Repeated failed non-invasive prenatal testing in a woman with immune thrombocytopenia and antiphospholipid syndrome: lessons learnt.Clinical Utility of Non-Invasive Prenatal Screening from Maternal Blood.Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testingSize-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.The Epigenome View: An Effort towards Non-Invasive Prenatal DiagnosisA new model for providing cell-free DNA and risk assessment for chromosome abnormalities in a public hospital settingDNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.Combined first-trimester screening in northern Finland: experiences of the first ten years.Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohortAssessment of Foetal DNA in Maternal Blood - A Useful Tool in the Hands of Prenatal Specialists.Genomics and perinatal care
P2860
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P2860
Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Non-invasive prenatal assessme ...... g: large scale validity study.
@ast
Non-invasive prenatal assessme ...... g: large scale validity study.
@en
Non-invasive prenatal assessme ...... g: large scale validity study.
@nl
type
label
Non-invasive prenatal assessme ...... g: large scale validity study.
@ast
Non-invasive prenatal assessme ...... g: large scale validity study.
@en
Non-invasive prenatal assessme ...... g: large scale validity study.
@nl
prefLabel
Non-invasive prenatal assessme ...... g: large scale validity study.
@ast
Non-invasive prenatal assessme ...... g: large scale validity study.
@en
Non-invasive prenatal assessme ...... g: large scale validity study.
@nl
P2093
P2860
P50
P356
P1433
P1476
Non-invasive prenatal assessme ...... g: large scale validity study.
@en
P2093
Attie T J I Go
Cees B M Oudejans
Elizabeth T Lau
Fiona M F Lun
Helena Lam
John M G van Vugt
K C Allen Chan
Kypros H Nicolaides
Mary H Y Tang
Ranjit Akolekar
P2860
P356
10.1136/BMJ.C7401
P407
P577
2011-01-11T00:00:00Z