Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
about
Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracyNoninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociNon-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issuesFalse Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature ReviewCracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesNew 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 ProspectsPerinatal systemic gene delivery using adeno-associated viral vectorsNon-invasive prenatal testing: a review of international implementation and challengesIdentification of trisomy 18, trisomy 13, and Down syndrome from maternal plasmaNon-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single centerNoninvasive 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-analysisIncorporating DNA sequencing into current prenatal screening practice for Down's syndromeFAST-SeqS: a simple and efficient method for the detection of aneuploidy by massively parallel sequencingNoninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNALimitations of Aneuploidy and Anomaly Detection in the Obese Patient.Decision aids that support decisions about prenatal testing for Down syndrome: an environmental scan.Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Aneuploidy screening by non-invasive prenatal testing in twin pregnancyNoninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencingImprovements in antenatal screening for Down's syndrome.Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.Noninvasive prenatal diagnosis in a fetus at risk for methylmalonic acidemia.Impact of prenatal screening on the prevalence of Down syndrome in SloveniaA new model for providing cell-free DNA and risk assessment for chromosome abnormalities in a public hospital settingAttitudes of mothers of children with down syndrome towards noninvasive prenatal testing.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.Non-invasive prenatal measurement of the fetal genomeFrom prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples.What women want: lead considerations for current and future applications of noninvasive prenatal testing in prenatal careGestational age and maternal weight effects on fetal cell-free DNA in maternal plasma.Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencingHigh resolution size analysis of fetal DNA in the urine of pregnant women by paired-end massively parallel sequencing
P2860
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P2860
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
description
2012 nî lūn-bûn
@nan
2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@ast
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@en
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@nl
type
label
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@ast
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@en
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@nl
prefLabel
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@ast
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@en
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@nl
P2093
P1476
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
@en
P2093
Alfred Z Abuhamad
Amy J Sehnert
Diana W Bianchi
James D Goldberg
Lawrence D Platt
MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group
Richard P Rava
P304
P356
10.1097/AOG.0B013E31824FB482
P407
P577
2012-05-01T00:00:00Z