Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
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 issuesNon-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 ProspectsTracking fetal development through molecular analysis of maternal biofluidsNoninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementDown Syndrome: Current Status, Challenges and Future PerspectivesMaternal plasma and amniotic fluid sphingolipids profiling in fetal Down syndromeFAST-SeqS: a simple and efficient method for the detection of aneuploidy by massively parallel sequencingLimitations of Aneuploidy and Anomaly Detection in the Obese Patient.Copy-number variation and false positive prenatal aneuploidy screening results.Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testingNovel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.The first 3,000 Non-Invasive Prenatal Tests (NIPT) with the Harmony test in Belgium and the Netherlands.A new model for providing cell-free DNA and risk assessment for chromosome abnormalities in a public hospital settingElevated levels of circulating DNA in cardiovascular disease patients: metagenomic profiling of microbiome in the circulation.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.From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Recent advances in the prenatal interrogation of the human fetal genome.Gestational 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.High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasmaMethods for multiplex template sampling in digital PCR assays"Don't Want No Risk and Don't Want No Problems": Public Understandings of the Risks and Benefits of Non-Invasive Prenatal Testing in the United StatesAnalysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.Detection of fetal cell-free DNA in maternal plasma for Down syndrome, Edward syndrome and Patau syndrome of high risk fetusNon-invasive prenatal diagnosis by massively parallel sequencing of maternal plasma DNA.Prenatal diagnosis of a 46,XX male following noninvasive prenatal testing.Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy.Brief Communication: Maternal Plasma Autoantibodies Screening in Fetal Down Syndrome.Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road?Circulating nucleic acids in plasma and serum: applications in diagnostic techniques for noninvasive prenatal diagnosis.Non-invasive Prenatal Testing: Technologies, Clinical Assays and Implementation Strategies for Women's Healthcare Practitioners.Noninvasive screening tools for Down syndrome: a review.Recent advances of genomic testing in perinatal medicine
P2860
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P2860
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@ast
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@en
type
label
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@ast
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@en
prefLabel
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@ast
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@en
P2093
P2860
P356
P1433
P1476
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
@en
P2093
Andrew B Sparks
Aoy Tomita-Mitchell
Arnold Oliphant
Celeste McBride
Craig A Struble
Desiree Hollemon
Eric T Wang
Jacob Zahn
Jay Sandler
Jigna Doshi
P2860
P356
10.1002/PD.2922
P577
2012-01-06T00:00:00Z