Measuring the strength of associations between HLA antigens and diseases.
about
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type IIIRecent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.Age estimate of the N370S mutation causing Gaucher disease in Ashkenazi Jews and European populations: A reappraisal of haplotype data.Identifying the susceptibility gene(s) in a set of trait-linked genes using genotype data.Population relationships in the Mediterranean revealed by autosomal genetic data (Alu and Alu/STR compound systems).Genetic susceptibility to early onset pauciarticular juvenile chronic arthritis: a study of HLA and complement markers in 158 British patients.MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.MHC polymorphism and disease resistance to Vibrio anguillarum in 8 families of half-smooth tongue sole (Cynoglossus semilaevis).Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis.Localization of a small genomic region associated with elevated ACEPrimarily chronic progressive and relapsing/remitting multiple sclerosis: two immunogenetically distinct disease entities.Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.The USH2A c.2299delG mutation: dating its common origin in a Southern European population.A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.Search for a founder mutation in idiopathic focal dystonia from Northern GermanyDisequilibrium mapping of a quantitative-trait locus in an expanding population.Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutationsPopulation distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649).DR and non-DR Ia allotypes are associated with susceptibility to coeliac diseaseBalancing selection at closely linked, overdominant loci in a finite population.Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium.Linkage disequilibrium--understanding the evolutionary past and mapping the medical future.Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas.The use of association data to identify family members at high risk for marker-linked diseases.Genetic heterogeneity of insulin-dependent (type I) diabetes mellitus: evidence from a study of extended haplotypesHaplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomesCharacterisation of patients with primary biliary cirrhosis responding to long term ursodeoxycholic acid treatmentAncestral association between HLA and HFE H63D and C282Y gene mutations from northwest Colombia.Are moment bounds on the recombination fraction between a marker and a disease locus too good to be true? Allelic association mapping revisited for simple genetic diseases in the Finnish populationHaplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of RussiaFamily-based association tests for different family structures using pooled DNACharacterizing linkage disequilibrium in pig populations.Exchangeable models of complex inherited diseasesHuman leukocyte antigen-b27 and disease susceptibility in vojvodina, serbia.Breed distribution and history of canine mdr1-1Delta, a pharmacogenetic mutation that marks the emergence of breeds from the collie lineageEnhancing the power to detect low-frequency variants in genome-wide screens.Pediatric and adult forms of type I autoimmune hepatitis in Argentina: evidence for differential genetic predisposition.Leprosy in a high-prevalence Egyptian village: epidemiology and risk factors.A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect.
P2860
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P2860
Measuring the strength of associations between HLA antigens and diseases.
description
1981 nî lūn-bûn
@nan
1981 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1981 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
name
Measuring the strength of associations between HLA antigens and diseases.
@ast
Measuring the strength of associations between HLA antigens and diseases.
@en
Measuring the strength of associations between HLA antigens and diseases.
@nl
type
label
Measuring the strength of associations between HLA antigens and diseases.
@ast
Measuring the strength of associations between HLA antigens and diseases.
@en
Measuring the strength of associations between HLA antigens and diseases.
@nl
prefLabel
Measuring the strength of associations between HLA antigens and diseases.
@ast
Measuring the strength of associations between HLA antigens and diseases.
@en
Measuring the strength of associations between HLA antigens and diseases.
@nl
P1433
P1476
Measuring the strength of associations between HLA antigens and diseases.
@en
P2093
Bengtsson BO
P304
P356
10.1111/J.1399-0039.1981.TB01404.X
P577
1981-11-01T00:00:00Z