Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry. - Wikidata - wikimedia - TriplyDB

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

http://www.wikidata.org/entity/Q33263753

about

A rapid and accurate approach to identify single nucleotide polymorphisms of mitochondrial DNA using MALDI-TOF mass spectrometry.MALDI-TOF MS in Prenatal Genomics.Current and Emerging Technologies for the Analysis of the Genome-Wide and Locus-Specific DNA Methylation Patterns.Prenatal diagnosis of fetal aneuploidies: post-genomic developments.Prenatal diagnosis of trisomy 21 by quantitatively pyrosequencing heterozygotes using amniotic fluid as starting material of PCR.

P2860

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P2860

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

http://www.wikidata.org/entity/Q33263753

description

2006 nî lūn-bûn

@nan

2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2006年の論文

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2006年論文

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2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@ast

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@en

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@nl

type

label

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@ast

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@en

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@nl

prefLabel

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@ast

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@en

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@nl

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P1433

Genetics in Medicine

P1476

Reliable detection of trisomy 21 using MALDI-TOF mass spectrometry.

@en

P2093

Balint Nagy

http://www.w3.org/2001/XMLSchema#string

Bernhard Zimmermann

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Dorothy J Huang

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Friedel Wenzel

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Lech Dudarewicz

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Matthew R Nelson

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Roland Spiegel

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Sinuhe Hahn

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Wolfgang Holzgreve

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P2860

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities.

Down syndrome phenotypes: the consequences of chromosomal imbalance.

Rapid trisomy diagnosis (21, 18, and 13) using fluorescent PCR and short tandem repeats: applications for prenatal diagnosis and preimplantation genetic diagnosis

Comparative genomic hybridization and prenatal diagnosis.

Origin and mechanisms of non-disjunction in human autosomal trisomies.

Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sex.

Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

Rapid determination of trisomy 21 from amniotic fluid cells using single-nucleotide polymorphic loci.

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728-734

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scholarly article

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11

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8

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6688647

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1032584150

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17108765

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P921

matrix-assisted laser desorption/ionization