A comparison of linkage disequilibrium measures for fine-scale mapping.
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Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variantsChapter 11: Genome-wide association studiesARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFTNF polymorphisms modify endotoxin exposure-associated longitudinal lung function declineGenetic variation in genes associated with arsenic metabolism: glutathione S-transferase omega 1-1 and purine nucleoside phosphorylase polymorphisms in European and indigenous Americans.Genetic signatures of strong recent positive selection at the lactase gene.Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetesWidespread genetic exchange among terrestrial bacteriophages.Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association.Developmentally restricted genetic determinants of human arsenic metabolism: association between urinary methylated arsenic and CYT19 polymorphisms in children.A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.Genetic variation in the 22q11 locus and susceptibility to schizophreniaAssociation between genetic polymorphisms of the beta2-adrenoceptor and response to albuterol in children with and without a history of wheezingPhosphodiesterase 4D and 5-lipoxygenase activating protein genes and risk of ischemic stroke in SardiniansA weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levelsComplete sequencing shows a role for MSX1 in non-syndromic cleft lip and palateComprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.Patterns of linkage disequilibrium and haplotype distribution in disease candidate genesOestrogen receptor alpha gene haplotype and postmenopausal breast cancer risk: a case control studyGenetic polymorphisms in the matrix metalloproteinase 12 gene (MMP12) and breast cancer risk and survival: the Shanghai Breast Cancer Study.SNPAnalyzer: a web-based integrated workbench for single-nucleotide polymorphism analysisEvidence of a large-scale functional organization of mammalian chromosomesInferring haplotypes at the NAT2 locus: the computational approach.Comprehensive search for intra- and inter-specific sequence polymorphisms among coding envelope genes of retroviral origin found in the human genome: genes and pseudogenes.JLIN: a java based linkage disequilibrium plotter.The Development of Quality Control Genotyping Approaches: A Case Study Using Elite Maize LinesPolymorphisms of prostaglandin-endoperoxide synthase 2 gene, and prostaglandin-E receptor 2 gene, C-reactive protein concentrations and risk of atherothrombosis: a nested case-control approachAssociation of GABRG3 with alcohol dependenceSupport for EKN1 as the susceptibility locus for dyslexia on 15q21Common sequence variants in pharmacodynamic and pharmacokinetic pathway-related genes conferring LDL cholesterol response to statinsADH4 gene variation is associated with alcohol dependence and drug dependence in European Americans: results from HWD tests and case-control association studiesSpontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variantsGenetic background of patients from a university medical center in Manhattan: implications for personalized medicinePopulation structure and evolution of RhinovirusesA Common Susceptibility Gene for Type 2 Diabetes Is Associated with Drug Response to a DPP-4 Inhibitor: Pharmacogenomic Cohort in Okinawa JapanAblation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice.The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination.Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibriumScreening of Genetic Polymorphisms of CYP3A4 and CYP3A5 Genes.
P2860
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P2860
A comparison of linkage disequilibrium measures for fine-scale mapping.
description
1995 nî lūn-bûn
@nan
1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
A comparison of linkage disequilibrium measures for fine-scale mapping.
@ast
A comparison of linkage disequilibrium measures for fine-scale mapping.
@en
A comparison of linkage disequilibrium measures for fine-scale mapping.
@nl
type
label
A comparison of linkage disequilibrium measures for fine-scale mapping.
@ast
A comparison of linkage disequilibrium measures for fine-scale mapping.
@en
A comparison of linkage disequilibrium measures for fine-scale mapping.
@nl
prefLabel
A comparison of linkage disequilibrium measures for fine-scale mapping.
@ast
A comparison of linkage disequilibrium measures for fine-scale mapping.
@en
A comparison of linkage disequilibrium measures for fine-scale mapping.
@nl
P356
P1433
P1476
A comparison of linkage disequilibrium measures for fine-scale mapping.
@en
P2093
P304
P356
10.1006/GENO.1995.9003
P577
1995-09-01T00:00:00Z