Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
about
Non-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsNon-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohortAn Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population.Digynic triploidy: utility and challenges of noninvasive prenatal testingCirculating Cell Free DNA in the Diagnosis of Trophoblastic TumorsSingle Nucleotide Polymorphism-Based Analysis of Cell-Free Fetal DNA in 3000 Cases from Germany and AustriaClinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.Comparative study of single-nucleotide polymorphism array and next generation sequencing based strategies on triploid identification in preimplantation genetic diagnosis and screen.Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.Cell-free DNA versus intact fetal cells for prenatal genetic diagnostics: what does the future hold?Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNABenefits and limitations of prenatal screening for Prader-Willi syndrome.Noninvasive prenatal testing for aneuploidy using cell-free DNA - New implications for maternal health.The potential impact of NIPT as a second-tier screen on the outcomes of high-risk pregnancies with rare chromosomal abnormalities.Adverse perinatal outcomes are more frequent in pregnancies with a low fetal fraction result on noninvasive prenatal testing.Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.Comment on "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods".Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.Should cell-free fetal DNA be included in first trimester screening (FTS) for common trisomy? A possible scenario on 6697 women screened over 10 years.
P2860
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P2860
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
description
2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@ast
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@en
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@nl
type
label
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@ast
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@en
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@nl
prefLabel
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@ast
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@en
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@nl
P2093
P356
P1476
Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood.
@en
P2093
Kypros H Nicolaides
Maria Soledad Quezada
Maria del Mar Gil
Yana Zinevich
P304
P356
10.1159/000355655
P577
2013-10-10T00:00:00Z