(Q48068018)

8 February 2018

title

Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE). (English)

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8 February 2018

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linkage disequilibrium

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G Gandon

1

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8 February 2018

A M Jouanolle

2

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8 February 2018

B Chauvel

3

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8 February 2018

V Mauvieux

4

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8 February 2018

A le Treut

5

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8 February 2018

J Feingold

6

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8 February 2018

J Y Le Gall

7

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8 February 2018

V David

8

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8 February 2018

J Yaouanq

9

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8 February 2018

publication date

1 January 1996

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8 February 2018

published in

Human Genetics

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8 February 2018

volume

97

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8 February 2018

issue

1

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8 February 2018

page(s)

103-113

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8 February 2018

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease

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Heterogeneity in disease associations

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Genetics of hemochromatosis: HLA association and mode of inheritance

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

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The effect of combining alleles into electrophoretic classes on detecting linkage disequilibrium

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Alleles at D6S265 and D6S105 define a haemochromatosis-specific genotype

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Is all genetic (hereditary) hemochromatosis HLA-associated

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

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Major histocompatibility complex (MHC) complement deficiency, ancestral haplotypes and systemic lupus erythematosus (SLE): C4 deficiency explains some but not all of the influence of the MHC.

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Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)

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Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis

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

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Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.

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Mapping and characterization of non-HLA multigene assemblages in the human MHC class I region

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Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity

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Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis

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DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family

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Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information

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Cloning and physical mapping of the HLA class I region spanning the HLA-E-to-HLA-F interval by using yeast artificial chromosomes

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Two polymorphisms at the locus D698 defined by a YAC.

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Isolation of novel non-HLA gene fragments from the hemochromatosis region (6p21.3) by cDNA hybridization selection

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Linkage disequilibrium in finite populations

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Physical and genetic mapping of the telomeric major histocompatibility complex region in man and relevance to the primary hemochromatosis gene (HFE).

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Identification of the cystic fibrosis gene: genetic analysis

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Maximum-likelihood estimation of gene location by linkage disequilibrium

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Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6

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A new polymorphic porbe close to HLA-A

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Testing Hypotheses about Linkage Disequilibrium with Multiple Alleles

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Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3.

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Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing

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Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

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A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

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Linkage disequilibrium among multiple neutral alleles produced by mutation in finite population

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12 December 2020

Measuring the strength of associations between HLA antigens and diseases

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12 December 2020

Isolation of CA dinucleotide repeats close to D6S105; linkage disequilibrium with haemochromatosis

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12 December 2020

DNA polymorphism and the study of disease associations

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12 December 2020

Class I gene contraction within the HLA-A subregion of the human MHC

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12 December 2020

Idiopathic hemochromatosis: significance and implications of linkage and association to HLA.

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Dinucleotide repeat polymorphism at the D6S510 locus

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12 December 2020

Recombination suppression of mouse t-haplotypes due to chromatin mismatching

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12 December 2020

Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F

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12 December 2020

A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA as

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12 December 2020

Differences in gene copy number carried by different MHC ancestral haplotypes. Quantitation after physical separation of haplotypes by pulsed field gel electrophoresis.

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12 December 2020

Identifiers

DOI

10.1007/BF00218843

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8 February 2018

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8 February 2018