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Search Results for: Hereditary Genetics

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  • Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet’s disease in Han Chinese
  • Association of tripartite motif family-like 2 (TRIML2) polymorphisms with late-onset Alzheimer’s disease risk in a Korean population
  • Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
  • Human Leukocyte Antigen-G Polymorphisms Association With Cancer Post-Heart Transplantation
  • Human leukocyte antigen G single-nucleotide polymorphism -201 (CC–CC) donor–recipient genotype matching as a predictor of severe cardiac allograft vasculopathy
  • Genetic susceptibility to dyslipidemia and incidence of cardiovascular disease depending on a diet quality index in the Malmö Diet and Cancer cohort
  • Several type 2 diabetes-associated variants in genes annotated to WNT signaling interact with dietary fiber in relation to incidence of type 2 diabetes
  • Further evidence for a parent-of-origin effect at the NOP9locus on language-related phenotypes
  • Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease-causing variants
  • Analysis of Rare Variants in the Alcohol Dependence Candidate GeneGATA4
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