DNA Sequencing versus Standard Prenatal Aneuploidy Screening
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A Balanced Look at the Implications of Genomic (and Other "Omics") Testing for Disease Diagnosis and Clinical CareNon-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issuesCracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesTrisomy 18 syndrome: Towards a balanced approachNon-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsToo much, too soon?: Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyondNon-invasive prenatal testing: a review of international implementation and challengesNoninvasive 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-analysisData collaboration will lead precision medicineAnalysis of Cell-Free DNA in Maternal Blood in Screening For Aneuploidies: Updated Meta-Analysis.The accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis.Copy-number variation and false positive prenatal aneuploidy screening results.Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessmentsNoninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing.Aneuploidy screening by non-invasive prenatal testing in twin pregnancyNoninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencingUtility of ultrasound examination at 10-14 weeks prior to cell-free DNA screening for fetal aneuploidy.Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.Establishment of a 10-Plex Quantitative Fluorescent-PCR Assay for rapid diagnosis of sex chromosome aneuploidies.The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform.Introducing the non-invasive prenatal test for trisomy 21 in Belgium: a cost-consequences analysisNoninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.The amniotic fluid transcriptome as a guide to understanding fetal disease.Noninvasive prenatal testing using cell-free fetal DNA in maternal plasma.Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral centerAn Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population.The Legal Past, Present and Future of Prenatal Genetic Testing: Professional Liability and Other Legal Challenges Affecting Patient Access to Services.Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18.Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis.Old Questions, New Paradigms: Ethical, Legal, and Social Complications of Noninvasive Prenatal Testing.A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection.Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes.The First Case Report in Italy of Di George Syndrome Detected by Noninvasive Prenatal Testing.Women's Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods StudyComparison of two high-throughput semiconductor chip sequencing platforms in noninvasive prenatal testing for Down syndrome in early pregnancyPositive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant WomenProof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations
P2860
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P2860
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@ast
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en-gb
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@nl
type
label
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@ast
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en-gb
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@nl
altLabel
DNA sequencing versus standard prenatal aneuploidy screening
@en
prefLabel
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@ast
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en-gb
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@nl
P2093
P3181
P356
P1476
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
@en
P2093
Amy J. Sehnert
Anita F. Das
Craig Saffer
Darya I. Chudova
Jeffrey Wentworth
Joseph A. Craig
Keith W. Jones
Kelly Oliver
Patricia L. Devers
R. Lamar Parker
P304
P3181
P356
10.1056/NEJMOA1311037
P407
P577
2014-02-27T00:00:00Z