(Q44126855)

30 November 2017

title

Haplotypic relationship between SNP and microsatellite markers at the NOS2A locus in two populations (English)

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30 November 2017

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1

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30 November 2017

Dominic P. Kwiatkowski

7

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30 November 2017

Rockett K

2

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30 November 2017

Ackerman H

3

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30 November 2017

Hull J

4

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30 November 2017

Usen S

5

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30 November 2017

Pinder M

6

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30 November 2017

publication date

1 October 2003

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30 November 2017

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30 November 2017

volume

4

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30 November 2017

issue

7

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30 November 2017

page(s)

506-514

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The future of genetic studies of complex human diseases

30 November 2017

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Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns

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Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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The critical region for Behçet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA-B, by association analysis using refined microsatellite mapping

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Significant association of longer forms of CCTTT Microsatellite repeat in the inducible nitric oxide synthase promoter with severe malaria in Thailand

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Minisatellite diversity supports a recent African origin for modern humans

21 January 2018

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Haplotype tagging for the identification of common disease genes

21 January 2018

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21 January 2018

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7 January 2021

Linkage disequilibrium mapping of complex disease: fantasy or reality?

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https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

A look at linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

The use of a genetic map of biallelic markers in linkage studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Nucleotide and haplotypic diversity of the NOS2A promoter region and its relationship to cerebral malaria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Genotyping and functional analysis of a polymorphic (CCTTT)(n) repeat of NOS2A in diabetic retinopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

(CCTTT)n repeat polymorphism in the NOS2 gene promoter is associated with atopy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Characterization and functional analysis of the human inducible nitric oxide synthase gene promoter.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364022

7 January 2021

Identifiers

DOI

10.1038/SJ.GENE.6364022

1 reference

release_sxlsnvh5tjgl3mz3lukmaecnqm

30 November 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/sxlsnvh5tjgl3mz3lukmaecnqm

24 November 2022

mapped directly with Wikidata item

1 reference