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  • Common genetic variations in cell cycle and DNA repair pathways associated with pediatric brain tumor susceptibility
  • Association Study of a Proliferation-inducing Ligand, Spermatogenesis Associated 8, Platelet-derived Growth Factor Receptor-alpha, and POLB Polymorphisms with Systemic Lupus Erythematosus in Chinese Han Population
  • Methylation and expression of PTPN22 in esophageal squamous cell carcinoma
  • An RGS2 3?UTR polymorphism is associated with preeclampsia in overweight women
  • Epigenetic changes in localized gastric cancer: the role of RUNX3 in tumor progression and the immune microenvironment
  • FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome
  • Positive selection of lactase persistence among people of Southern Arabia
  • Genetic variants of 20q12 contributed to non-syndromic orofacial clefts susceptibility
  • Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns
  • Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis.
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