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Article

Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues

30 Mar 2010

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 20350623
DOI: 10.1016/j.ejmg.2010.03.007

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Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissuesPMID 20350623Read ↗

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

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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Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18Semantic proximity Read ↗

Prenatal diagnosis of a familial 22q11.21 microduplication and mosaic trisomy 20 in a pregnancy with an asymptomatic father carrier and a favorable fetal outcomeSemantic proximity Read ↗

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Abnormal villous morphology associated with triple trisomy of paternal origin.Semantic proximity Read ↗

Biochemical Screening for Fetal Trisomy 21: Pathophysiology of Maternal Serum Markers and Involvement of the PlacentaSemantic proximity Read ↗

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