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1. ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1‐RUNX1T1 and associated with a better prognosis. Issue 5 (14th February 2017)

2. Impact of immunophenotypic characteristics on genetic subgrouping in childhood acute lymphoblastic leukemia: Tokyo Children's Cancer Study Group (TCCSG) study L04‐16. Issue 10 (16th July 2020)

3. Severe deep vein thrombosis and pulmonary embolism in a paediatric patient with primary antiphospholipid syndrome. Issue 1 (2nd January 2018)