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Search Results for: Hereditary Genetics

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  • Association between single-nucleotide polymorphism in Mal/TIRAP and Interleukin-10 genes and susceptibility to invasive Haemophilus influenzea serotype b infection in immunized children
  • FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies
  • Mutation screen and association study for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity
  • Allelic variants of IL1R1 gene associate with severe hand ostheoarthritis
  • Generalist genes analysis of DNA markers associated with mathematical ability and disability reveals shared influence across ages and abilities
  • Evaluating the association of common APOA2 variants with type 2 diabetes
  • Functional and genetic analysis in type 2 diabetes of liver X receptor alleles – a cohort study
  • Suggestive evidence of associations between liver X receptor beta polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT 2 (Norway), MONICA (France) and HELENA (Europe)
  • Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis
  • Polymorphisms in genes involved in the estrogen pathway and mammographic density
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