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Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31DOI 10.1136/jmg.40.10.792
Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31.Semantic proximity
Haplotype variation at the IBD5/SLC22A4 locus (5q31) in coeliac disease in the Irish population.Semantic proximity
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.Semantic proximity
Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.Semantic proximity
Role of the IBD5 susceptibility locus in the inflammatory bowel diseases.Semantic proximity
Genome-wide association scans identify multiple confirmed susceptibility loci for Crohn's disease: lessons for study design.Semantic proximity
The 5q31 variants associated with psoriasis and Crohn's disease are distinct.Semantic proximity
Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population.Semantic proximity
Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease.Semantic proximity
Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.Semantic proximity
Crohn's disease: genotype and phenotype considerations.Semantic proximity
Haplotype in the IBD5 region is associated with refractory Crohn's disease in Slovenian patients and modulates expression of the SLC22A5 gene.Semantic proximity
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