Non-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 center - Wikidata - wikimedia - TriplyDB

Non-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 center

Non-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 center

http://www.wikidata.org/entity/Q27007785

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Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.Copy-number variation and false positive prenatal aneuploidy screening results.Application of risk score analysis to low-coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13.Aneuploidy screening by non-invasive prenatal testing in twin pregnancy Six consecutive false positive cases from cell-free fetal DNA testing in a single referring centre The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform.Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.Comparison of two high-throughput semiconductor chip sequencing platforms in noninvasive prenatal testing for Down syndrome in early pregnancy Practicability of prenatal testing using lectin-based enrichment of fetal erythroblasts.Analysis of cell-free fetal DNA in maternal blood for detection of trisomy 21, 18 and 13 in a general pregnant population and in a high risk population - a systematic review and meta-analysis.Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation Fetal microchimerism and maternal health: a review and evolutionary analysis of cooperation and conflict beyond the womb.False Negative Cell-Free DNA Screening Result in a Newborn with Trisomy 13.Noninvasive prenatal testing in routine clinical practice for a high-risk population: Experience from a center.NIPTRIC: an online tool for clinical interpretation of non-invasive prenatal testing (NIPT) results.Clinical implementation of NIPT - technical and biological challenges.Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.Systematic review and meta-analysis of non-invasive prenatal DNA testing for trisomy 21: implications for implementation in China.The implications of non-invasive prenatal testing failures: a review of an under-discussed phenomenon.Benefits and limitations of prenatal screening for Prader-Willi syndrome.Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy.A population-based study of prevalence of Down syndrome in Southern Thailand.Validation of combinatorial probe-anchor ligation-based sequencing as non-invasive prenatal test for trisomy at a central laboratory.Identification of minor chromosomal defects causing abnormal foetus and spontaneous abortions.Noninvasive fetal trisomy detection by multiplexed semiconductor sequencing: a barcoding analysis strategy.Karyotype analysis with amniotic fluid in 12365 pregnant women with indications for genetic amniocentesis and strategies of prenatal diagnosis.Contingent non-invasive prenatal testing: an opportunity to improve non-genetic aspects of fetal aneuploidy screening.Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.Cell-free fetal DNA: the new tool in fetal medicine Combined first trimester screen or noninvasive prenatal testing or both.Clinical implementation of cell-free DNA-based aneuploidy screening: perspectives from a national audit.Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.Author's reply to Grati and Benn.Views of the obstetric profession on non-invasive prenatal testing in Aotearoa New Zealand: A national survey.Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?Screening for fetal chromosomal and subchromosomal disorders.

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Non-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 center

http://www.wikidata.org/entity/Q27007785

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P2860

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.

Is the prevalence of Klinefelter syndrome increasing?

Next-generation sequencing transforms today's biology.

Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities.

Clinical utility of noninvasive fetal trisomy (NIFTY) test--early experience.

Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma.

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