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  • CYP2C19 phenotype and body-weight-guided voriconazole initial dose in infants and children after hematopoietic cell transplantation
  • Cyclophosphamide bioactivation pharmacogenetics in breast cancer patients
  • Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
  • A validation study of the UGT1A4 rs2011404 variant and the risk of anti‐tuberculosis drug‐induced hepatotoxicity in an Eastern Chinese Han population
  • Influence of UGT2B7 and UGT1A6 polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic children
  • Rs3802278 in 3′-UTR of SULF1 associated with platinum resistance and survival in Chinese epithelial ovarian cancer patients
  • Resolving discordant CYP2D6 genotyping results in Thai: platform limitations and novel haplotypes
  • Polymorphisms in eicosanoid‐related biosynthesis enzymes associated with acute urticaria/angioedema induced by nonsteroidal anti‐inflammatory drug hypersensitivity
  • Association of polymorphism of CYP3A4, ABCB1, ABCC2, ABCG2, NFKB1, POR, and PXR with the concentration of cyclosporin a in allogeneic hematopoietic stem cell transplantation recipients
  • Pharmacogenetics of tenofovir and emtricitabine penetration into cerebrospinal fluid
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