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Search Results for: Hereditary Genetics

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  • Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy
  • Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease
  • Association between the dopamine transporter gene and the inattentive subtype of attention deficit hyperactivity disorder in Taiwan
  • Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms
  • CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guenea-Bisseau, West Africa
  • Characterization of 9p24 risk locus and colorectal adenoma and cancer; gene-environment interaction and meta-analysis
  • A population-based study of IGF axis polymorphisms and the esophageal inflammation, metaplasia, adenocarcinoma sequence
  • Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment
  • Investigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markers
  • Assessing association of common variation in the C1Q gene cluster with systemic lupus erythematosus
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