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Article

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

19 Feb 2011

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Share to Fetal and Pediatric Neurological Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 21310373
DOI: 10.1016/j.ajog.2010.12.060

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Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical settingPMID 21310373Read ↗

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical settingSemantic proximity Read ↗

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Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18Semantic proximity Read ↗

Non‐invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146 958 pregnanciesSemantic proximity Read ↗

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European Non‐Invasive Trisomy Evaluation (EU‐NITE) study: a multicenter prospective cohort study for non‐invasive fetal trisomy 21 testingSemantic proximity Read ↗

A robust second‐generation genome‐wide test for fetal aneuploidy based on shotgun sequencing cell‐free DNA in maternal bloodSemantic proximity Read ↗

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