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Search Results for: Hereditary Genetics

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  • Polymorphisms in stearoyl CoA desaturase and sterol regulatory element binding protein interact with N-3 polyunsaturated fatty acid intake to modify associations with anthropometric variables and metabolic phenotypes in Yup’ik people
  • Importance of nonsynonymous OCA2 variants in human eye color prediction
  • Effect of epidermal growth factor receptor gene polymorphisms on prognosis in glioma patients
  • Association analysis of ALOX5 gene polymorphisms with stroke risk: a case-control study in a Chinese Han population
  • A Case-Control study for Genetic Susceptibility Genes of Type 2 Diabetes with History of Obesity in Jordanian Population of Arab Descent
  • Association of CD59 and CFH polymorphisms with acute anterior uveitis in Chinese population
  • Association of NKAPL, TSPAN18, and MPC2 gene variants with schizophrenia based on new data and a meta-analysis in Han Chinese
  • Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet’s disease in Han Chinese
  • Association of GCH1 and MIR4697, but not SIPA1L2 andVPS13C polymorphisms, with Parkinson’s disease in Taiwan
  • Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
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