(Q81319536)

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Multiplex PCR-based real-time invader assay (mPCR-RETINA): a novel SNP-based method for detecting allelic asymmetries within copy number variation regions

scientific article published on 01 January 2008

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scholarly article

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7 January 2020

Multiplex PCR-based real-time invader assay (mPCR-RETINA): a novel SNP-based method for detecting allelic asymmetries within copy number variation regions (English)

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7 January 2020

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Michiaki Kubo

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7 January 2020

Yūsuke Nakamura

8

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Yusuke Nakamura

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7 January 2020

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Yozo Ohnishi

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7 January 2020

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Naoya Hosono

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7 January 2020

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Hiroko Sato

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7 January 2020

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Yumiko Tsuchiya

3

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7 January 2020

Takuya Kitamoto

5

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7 January 2020

Susumu Saito

6

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7 January 2020

publication date

1 January 2008

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7 January 2020

1 reference

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7 January 2020

29

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7 January 2020

1

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7 January 2020

182-189

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7 January 2020

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

1 reference

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Determination of cytochrome P450 2D6 (CYP2D6) gene copy number by real-time quantitative PCR.

1 reference

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Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease

1 reference

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Development of a PCR-based strategy for CYP2D6 genotyping including gene multiplication of worldwide potential use.

1 reference

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7 January 2021

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Copy number variation: new insights in genome diversity

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7 January 2021

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Codeine intoxication associated with ultrarapid CYP2D6 metabolism

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The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

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7 January 2021

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Detection of large-scale variation in the human genome

1 reference

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7 January 2021

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A haplotype map of the human genome

1 reference

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7 January 2021

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Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

1 reference

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7 January 2021

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Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene

1 reference

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7 January 2021

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Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes

1 reference

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7 January 2021

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A high-throughput SNP typing system for genome-wide association studies

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Lamin B1 duplications cause autosomal dominant leukodystrophy

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Global variation in copy number in the human genome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Large-scale copy number polymorphism in the human genome

1 reference

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7 January 2021

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inferred from DOI database lookup

Segmental duplications and copy-number variation in the human genome

1 reference

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7 January 2021

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Structural variation of the human genome

1 reference

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7 January 2021

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Diagnosis of alpha+-thalassemias by determining the ratio of the two alpha-globin gene copies by oligonucleotide hybridization and melting curve analysis

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Detection of Trisomy 21 by Quantitative Mass Spectrometric Analysis of Single-Nucleotide Polymorphisms

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7 January 2021

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Fine-scale structural variation of the human genome

1 reference

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7 January 2021

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High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays

1 reference

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Quantify single nucleotide polymorphism (SNP) ratio in pooled DNA based on normalized fluorescence real-time PCR

1 reference

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7 January 2021

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Identifiers

10.1002/HUMU.20609

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17879341%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17879341%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

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