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  • Comparative study on driver mutations in primary and metastatic melanomas at a single Japanese institute: A clue for intra-and inter-tumor heterogeneity
  • EGR2 mutations define a new clinically aggressive subgroup of chronic lymphocytic leukemia
  • Baseline and treatment-related changes in thrombin generation in patients with multiple myeloma
  • Integrated analysis of genome-wide DNA methylation and gene expression data provide a regulatory network in intrauterine growth restriction
  • EGFR T790M mutation testing within the osimertinib AURA Phase I study
  • Association of TGF-β3 and ANXA11 With Pulmonary Sarcoidosis in Greek Population
  • Technical Evaluation of Commercial Mutation Analysis Platforms and Reference Materials for Liquid Biopsy Profiling
  • Analysis of polymorphism and hepatic expression of duodenal cytochrome b in chronic hepatitis C
  • NT5C2 Gene Polymorphisms and the Risk of Coronary Heart Disease
  • DNA methylation and tag SNPs of the BDNF gene in conversion of amnestic mild cognitive impairment into Alzheimer’s disease: a cross-sectional cohort study
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