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Malignant pleural mesothelioma with an EML4-ALK fusion : expect the unexpected!
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Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms
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The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes
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Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone