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26. TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. Shurtleff SA; Buijs A; Behm FG; Rubnitz JE; Raimondi SC; Hancock ML; Chan GC; Pui CH; Grosveld G; Downing JR Leukemia; 1995 Dec; 9(12):1985-9. PubMed ID: 8609706 [TBL] [Abstract][Full Text] [Related]
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