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6. Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype. Kokate P; Ahmad F; Dalvi R; Das BR; Mandava S Cancer Genet Cytogenet; 2008 Jul; 184(1):52-6. PubMed ID: 18558290 [TBL] [Abstract][Full Text] [Related]
7. t(8;21)(q22;q22) Translocation involving AML1 and ETO in B lymphoblastic leukemia [corrected]. Wang HY; Tirado CA Hum Pathol; 2010 Feb; 41(2):286-92. PubMed ID: 19896694 [TBL] [Abstract][Full Text] [Related]
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10. Coexistent t(8;21)(q22;q22) Translocation and 5q Deletion in Acute Myeloid Leukemia. Yamamoto K; Yakushijin K; Sanada Y; Kawamoto S; Matsuoka H; Minami H J Clin Exp Hematop; 2015; 55(3):181-5. PubMed ID: 26763368 [TBL] [Abstract][Full Text] [Related]
11. Myeloid neoplasms with t(16;21)(q24;q22)/RUNX1-RUNX1T3 mimics acute myeloid leukemia with RUNX1-RUNX1T1. Liu H; Wang SA; Schlette EJ; Xu J; Jorgensen JL; Cameron Yin C; Li S; Jeffrey Medeiros L; Tang G Ann Hematol; 2018 Oct; 97(10):1775-1783. PubMed ID: 29872884 [TBL] [Abstract][Full Text] [Related]
13. Acute myeloid leukemia with t(8;21)(q22;q22.1)/RUNX1-RUNX1T1 and KIT Exon 8 mutation is associated with characteristic mastocytosis and dismal outcomes. Xie W; Wang SA; Yin CC; Xu J; Li S; Bueso-Ramos CE; Medeiros LJ; Tang G Exp Mol Pathol; 2019 Jun; 108():131-136. PubMed ID: 31004601 [TBL] [Abstract][Full Text] [Related]
14. Rearrangement of VPS13B, a causative gene of Cohen syndrome, in a case of RUNX1-RUNX1T1 leukemia with t(8;12;21). Abe A; Yamamoto Y; Katsumi A; Okamoto A; Tokuda M; Inaguma Y; Yamamoto K; Yanada M; Kanie T; Tomita A; Akatsuka Y; Okamoto M; Kameyama T; Mayeda A; Emi N Int J Hematol; 2018 Aug; 108(2):208-212. PubMed ID: 29264741 [TBL] [Abstract][Full Text] [Related]
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17. A Novel Translocation Involving RUNX1 and HOXA Gene Clusters in a Case of Acute Myeloid Leukemia with t(7;21)(p15;q22). Moon Y; Horsman DE; Humphries RK; Park G Immune Netw; 2013 Oct; 13(5):222-6. PubMed ID: 24198749 [TBL] [Abstract][Full Text] [Related]
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