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24. AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases. Schoch C; Schnittger S; Klaus M; Kern W; Hiddemann W; Haferlach T Blood; 2003 Oct; 102(7):2395-402. PubMed ID: 12805060 [TBL] [Abstract][Full Text] [Related]
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28. MLL genomic breakpoint distribution within the breakpoint cluster region in de novo leukemia in children. Felix CA; Hosler MR; Slater DJ; Parker RI; Masterson M; Whitlock JA; Rebbeck TR; Nowell PC; Lange BJ J Pediatr Hematol Oncol; 1998; 20(4):299-308. PubMed ID: 9703001 [TBL] [Abstract][Full Text] [Related]
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37. ABI-1, a human homolog to mouse Abl-interactor 1, fuses the MLL gene in acute myeloid leukemia with t(10;11)(p11.2;q23). Taki T; Shibuya N; Taniwaki M; Hanada R; Morishita K; Bessho F; Yanagisawa M; Hayashi Y Blood; 1998 Aug; 92(4):1125-30. PubMed ID: 9694699 [TBL] [Abstract][Full Text] [Related]
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