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  • Association of cytokine and toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
  • Common Genetic Variations in Patched1 (PTCH1) Gene and Risk of Hirschsprung Disease in the Han Chinese Populations
  • Association of maternal and nutrient supply line factors with DNA methylation at the imprinted IGF2/H19 locus in multiple tissues of newborn twins
  • Common Oncogenic Mutations Are Infrequent in Oral Squamous Cell Carcinoma of Asian Origin:
  • Association of polymorphisms in FLT3, EGFR, ALOX5, and NEIL3 with glioblastoma in the Han Chinese population
  • Comparison of SSR and SNP Markers in Estimation of Genetic Diversity and Population Structure of Indian Rice Varieties
  • Association of polymorphisms of potassium voltage-gated channel, KQT-like subfamily, member 1 and type 2 diabetes in Jiangsu province, China
  • Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma
  • Association of polymorphisms on chromosome 9p21.3 region with increased susceptibility of abdominal aortic aneurysm in a Chinese Han population
  • Association of promoter methylation of ERp57 gene with the pathogenesis of cervical lesions in Uighur women
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