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Oncotarget|March 25, 2016
Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progressionVito Alessandro Lasorsa, Daniela Formicola, Piero Pignataro, et al.Annals of Hematology|April 20, 2023
Efficacy and safety of nilotinib as frontline treatment in elderly (> 65 years) chronic myeloid leukemia patients outside clinical trialsLuigia Luciano, Roberto Latagliata, Gabriele Gugliotta, et al.Pediatric Blood & Cancer|May 1, 2015
Genetic abnormalities in adolescents and young adults with neuroblastoma: A report from the Italian Neuroblastoma groupKatia Mazzocco, Raffaella Defferrari, Angela Rita Sementa, et al.Nature Genetics|June 30, 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type IIKlaus Schwarz, Achille Iolascon, Fatima Verissimo, et al.Blood|March 13, 2013
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1Immacolata Andolfo, Seth L Alper, Lucia De Franceschi, et al.Pageof 4