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Search Results for: Hereditary Genetics

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  • Association between single nucleotide polymorphism of transforming growth factor β1 gene rs2317130 and susceptibility to tuberculosis.
  • An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
  • Using the optimal method—explained variance weighted genetic risk score to predict the efficacy of folic acid therapy to hyperhomocysteinemia
  • Polymorphisms in the mTOR-PI3K-Akt pathway, energy balance-related exposures and colorectal cancer risk in the Netherlands Cohort Study
  • TIMP2 genetic variation rs4789932 may associate with an increased risk of developing acne scarring based on a case‐control study of Chinese Han population
  • Contributions of common genetic variants to specific languages and to when a language is learned
  • Risk Stratification for Early-Onset Colorectal Cancer Using a Combination of Genetic and Environmental Risk Scores: An International Multi-Center Study
  • The common rs13266634 C> T variant in SLC30A8 contributes to the heterogeneity of phenotype and clinical features of both type 1 and type 2 diabetic subtypes
  • Association Between SNPs in the One-Carbon Metabolism Pathway and the Risk of Female Breast Cancer in a Chinese Population
  • Flow Cytometry Identifies an Early Stage of Platelet Apoptosis Produced by Agonists of the P2X1 and P2X7 Receptors
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