Improving enrichment of circulating fetal DNA for genetic testing: size fractionation followed by whole gene amplification - sprookjes - yvandenbroek - TriplyDB

Improving enrichment of circulating fetal DNA for genetic testing: size fractionation followed by whole gene amplification

Improving enrichment of circulating fetal DNA for genetic testing: size fractionation followed by whole gene amplification

http://www.wikidata.org/entity/Q33621782

about

Towards standardisation of cell-free DNA measurement in plasma: controls for extraction efficiency, fragment size bias and quantification Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms Fragment size analysis of free fetal DNA in maternal plasma using Y-STR loci and SRY gene amplification.Size-selective separation and overall-amplification of cell-free fetal DNA fragments using PCR-based enrichment.Cell-free Fetal Nucleic Acid Identifier Markers in Maternal Circulation.Epigenetic biomarkers: Current strategies and future challenges for their use in the clinical laboratory.Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment.

P2860

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P2860

Improving enrichment of circulating fetal DNA for genetic testing: size fractionation followed by whole gene amplification

http://www.wikidata.org/entity/Q33621782

description

2009 nî lūn-bûn

@nan

2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Improving enrichment of circul ...... ed by whole gene amplification

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Improving enrichment of circul ...... ed by whole gene amplification

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Fetal Diagnosis and Therapy

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Improving enrichment of circul ...... ed by whole gene amplification

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P2093

Carolina J Jorgez

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Farideh Z Bischoff

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P2860

Non-invasive prenatal detection of achondroplasia in size-fractionated cell-free DNA by MALDI-TOF MS assay.

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

Cell-free fetal DNA and intact fetal cells in maternal blood circulation: implications for first and second trimester non-invasive prenatal diagnosis.

Cell-free fetal DNA in maternal blood: kinetics, source and structure.

Fetal cells and cell free fetal nucleic acids in maternal blood: new tools to study abnormal placentation?

Hypoxia-induced membrane-bound apoptotic DNA particles: potential mechanism of fetal DNA in maternal plasma.

Detecting fetal DNA from dried maternal blood spots: another step towards broad scale non-invasive prenatal genetic screening and feasible testing.

Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms.

Size distributions of maternal and fetal DNA in maternal plasma.

Maternal plasma fetal DNA as a marker for preterm labour.

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314-319

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scholarly article

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10.1159/000235877

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3

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25

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2009-09-22T00:00:00Z

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26833665

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19776594

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2814146

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