Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region. (Q41452308)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7913583%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region (English)

1 reference

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28 October 2019

1 reference

linkage disequilibrium

1 reference

W S Watkins

1

1 reference

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28 October 2019

R Zenger

2

1 reference

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28 October 2019

E O'Brien

3

1 reference

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28 October 2019

D Nyman

4

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28 October 2019

A W Eriksson

5

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28 October 2019

M Renlund

6

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28 October 2019

L B Jorde

7

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28 October 2019

language of work or name

English

0 references

publication date

1 August 1994

1 reference

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American Journal of Human Genetics

28 October 2019

published in

1 reference

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28 October 2019

volume

55

1 reference

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28 October 2019

issue

2

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28 October 2019

page(s)

348-355

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Testing Hypotheses about Linkage Disequilibrium with Multiple Alleles

28 October 2019

cites work

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30 September 2017

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Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene

30 September 2017

1 reference

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Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites

30 September 2017

1 reference

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Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.

30 September 2017

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Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping

30 September 2017

1 reference

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Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization

30 September 2017

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Polymorphic DNA region adjacent to the 5' end of the human insulin gene

30 September 2017

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30 September 2017

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Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q.

30 September 2017

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A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. I. Basic theory and an analysis of alcohol dehydrogenase activity in Drosophila

30 September 2017

1 reference

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Structure of the gene for human von Willebrand factor

30 September 2017

1 reference

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Identification of the cystic fibrosis gene: genetic analysis

30 September 2017

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Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

30 September 2017

1 reference

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Polymorphic DNA haplotypes at the LDL receptor locus

30 September 2017

1 reference

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Tetranucleotide repeat polymorphism in the vWF gene

30 September 2017

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The von Willebrand factor gene and genetics of von Willebrand's disease

30 September 2017

1 reference

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Molecular biology of von Willebrand factor

30 September 2017

1 reference

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RsaI polymorphism in von Willebrand factor (vWF) at codon 789.

30 September 2017

1 reference

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Linkage disequilibrium between two highly polymorphic microsatellites.

30 September 2017

1 reference

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Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination

30 September 2017

1 reference

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Complex patterns of linkage disequilibrium in the Huntington disease region

30 September 2017

1 reference

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Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis.

30 September 2017

1 reference

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A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates

30 September 2017

1 reference

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Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene

30 September 2017

1 reference

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Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1

30 September 2017

1 reference

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Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I

30 September 2017

1 reference

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Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population

30 September 2017

1 reference

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Linkage disequilibrium among RFLPs at the insulin-receptor locus despite intervening Alu repeat sequences

30 September 2017

1 reference

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A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age

30 September 2017

1 reference

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Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.

30 September 2017

1 reference

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Digitized and differentially shaded human chromosome ideograms for genomic applications.

11 June 2018

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Maximum-likelihood estimation of gene location by linkage disequilibrium

11 June 2018

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Linkage disequilibrium and homozygosity of chromosome segments in finite populations

11 June 2018

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Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918364

Population size bottleneck.

11 June 2018

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Linkage disequilibrium between DNA markers at the low-density lipoprotein receptor gene.

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918364

Construction of a GT polymorphism map of human 9q

11 June 2018

1 reference

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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

11 June 2018

1 reference

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A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of th

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918364

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918364

von Willebrand disease: a database of point mutations, insertions, and deletions. For the Consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7913583

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7913583%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference