(Q46087295)

19 December 2017

title

Candidate gene copy number analysis by PCR and multicapillary electrophoresis (English)

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19 December 2017

author name string

Eszter Szantai

1

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19 December 2017

Zsuzsanna Elek

2

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19 December 2017

András Guttman

3

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19 December 2017

Maria Sasvari-Szekely

4

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19 December 2017

publication date

1 April 2009

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19 December 2017

published in

Electrophoresis

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19 December 2017

volume

30

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19 December 2017

issue

7

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19 December 2017

page(s)

1098-1101

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19 December 2017

Structural variation in the human genome

cites work

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Polymorphisms in the hypoxia inducible factor-1alpha gene (HIF1A) are associated with the renal cell carcinoma phenotype

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

No direct effect of the -521 C/T polymorphism in the human dopamine D4 receptor gene promoter on transcriptional activity

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

A genetic polymorphism in the promoter region of DRD4 associated with expression and schizophrenia.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Copy number variation: new insights in genome diversity

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Increase inGSK3β gene copy number variation in bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Real-time PCR quantification of human complement C4A and C4B genes

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Rapid quantification of human complement component C4A and C4B genes by capillary gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800755

7 January 2021

Identifiers

DOI

10.1002/ELPS.200800755

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19 December 2017

1 reference

19 December 2017