Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach.
about
Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012Non-invasive prenatal diagnosis of fetal trisomy 21 using cell-free fetal DNA in maternal bloodFree DNA--new potential analyte in clinical laboratory diagnostics?Applicability of digital PCR to the investigation of pediatric-onset genetic disordersHigh-throughput droplet digital PCR system for absolute quantitation of DNA copy numberNoninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencingThe accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis.Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testingDetection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome.Epigenetic-genetic chromosome dosage approach for fetal trisomy 21 detection using an autosomal genetic reference marker.The Epigenome View: An Effort towards Non-Invasive Prenatal DiagnosisFetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21.The triple test as a screening technique for Down syndrome: reliability and relevance.Six consecutive false positive cases from cell-free fetal DNA testing in a single referring centreDNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples.Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosisNon-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.Epigenetic approaches for the detection of fetal DNA in maternal plasma.Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?Discovery of epigenetic biomarkers for the noninvasive diagnosis of fetal disease.Quantification of epigenetic biomarkers: an evaluation of established and emerging methods for DNA methylation analysisWhole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domains.Microarray-Based Analysis of Methylation Status of CpGs in Placental DNA and Maternal Blood DNA--Potential New Epigenetic Biomarkers for Cell Free Fetal DNA-Based Diagnosis.Bisulfite Conversion of DNA: Performance Comparison of Different Kits and Methylation Quantitation of Epigenetic Biomarkers that Have the Potential to Be Used in Non-Invasive Prenatal Testing.Microarray-Based Analysis of Methylation of 1st Trimester Trisomic Placentas from Down Syndrome, Edwards Syndrome and Patau SyndromeNon-invasive prenatal diagnosis using cell-free fetal nucleic acids in maternal plasma: Progress overview beyond predictive and personalized diagnosisNon-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.Non invasive prenatal diagnosis of aneuploidy: next generation sequencing or fetal DNA enrichment?A new method for non-invasive prenatal diagnosis of Down syndrome using MeDIP real time qPCR.Current controversies in prenatal diagnosis 2: Down syndrome screening: is ultrasound better than cell-free nucleic acids in maternal blood?DNA methylation profiling highlights the unique nature of the human placental epigenome.Noninvasive prenatal diagnosis empowered by high-throughput sequencing.Noninvasive prenatal diagnosis of monogenic disorders.Non-invasive prenatal testing for aneuploidy: current status and future prospects.Role of the second-trimester 'genetic sonogram' for Down syndrome screen in the era of first-trimester screening and noninvasive prenatal testing.Cell-free Fetal Nucleic Acid Identifier Markers in Maternal Circulation.Three-color crystal digital PCR.Prenatal diagnosis of fetal aneuploidies: post-genomic developments.Noninvasive fetal trisomy detection by multiplexed semiconductor sequencing: a barcoding analysis strategy.
P2860
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P2860
Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Noninvasive prenatal detection ...... ic chromosome-dosage approach.
@en
Noninvasive prenatal detection ...... ic chromosome-dosage approach.
@nl
type
label
Noninvasive prenatal detection ...... ic chromosome-dosage approach.
@en
Noninvasive prenatal detection ...... ic chromosome-dosage approach.
@nl
prefLabel
Noninvasive prenatal detection ...... ic chromosome-dosage approach.
@en
Noninvasive prenatal detection ...... ic chromosome-dosage approach.
@nl
P2093
P1433
P1476
Noninvasive prenatal detection ...... tic chromosome-dosage approach
@en
P2093
Chunming Ding
K C Allen Chan
Rossa W K Chiu
Shengnan Jin
Tak Y Leung
Y M Dennis Lo
P356
10.1373/CLINCHEM.2009.134114
P407
P50
P577
2009-10-22T00:00:00Z