Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing? - Wikidata - awgldk - TriplyDB

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?

http://www.wikidata.org/entity/Q41260566

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Spanish- and English-Speaking Pregnant Women's Views on cfDNA and Other Prenatal Screening: Practical and Ethical Reflections.Has Noninvasive Prenatal Testing (NIPT) Come of Age?Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.Genomic futures of prenatal screening: ethical reflection.Nuchal translucency distributions for different chromosomal anomalies in a large unselected population cohort.Comparison of first-tier cell-free DNA screening for common aneuploidies with conventional publically funded screening.The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.Nuchal translucency measurement in the era of prenatal screening for aneuploidy using cell free (cf)DNA.Prenatal screening for genetic disorders: Suggested guidelines for the Indian Scenario.Current controversies in prenatal diagnosis 3: is there still a value in a nuchal translucency screening ultrasound in conjunction with maternal plasma non-invasive cell-free DNA testing?

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Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?

http://www.wikidata.org/entity/Q41260566

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Detection of fetal chromosomal ...... non-invasive prenatal testing?

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Detection of fetal chromosomal ...... non-invasive prenatal testing?

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Detection of fetal chromosomal ...... non-invasive prenatal testing?

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Prenatal Diagnosis

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Detection of fetal chromosomal ...... non-invasive prenatal testing?

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B D M Diemel

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G C M L Page-Christiaens

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G H Schuring-Blom

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G T R Manten

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J Siljee

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K D Lichtenbelt

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M P H Koster

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P2860

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

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

Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss.

Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior, and fertility.

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

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.

Relation between increased fetal nuchal translucency thickness and chromosomal defects.

Explaining variation in Down's syndrome screening uptake: comparing the Netherlands with England and Denmark using documentary analysis and expert stakeholder interviews.

Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.

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663-668

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10.1002/PD.4589

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7

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35

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2015-04-10T00:00:00Z

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