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- [21] Complex Karyotype but Not Blast Percentage Is Associated with Poor Survival in Acute Myeloid Leukemia and Myelodysplastic Syndrome with Inv(3)(q21q26.2)/t(3;3)(q21;q26.2); a Bone Marrow Pathology Group StudyLABORATORY INVESTIGATION, 2013, 93 : 358A - 358ARogers, H. J.Vardiman, J. W.Anastasi, J.Raca, G.Savage, N. M.Cherry, A. M.Arber, D.Moore, E.Morrissette, J. J. D.Bagg, A.Liu, Y-CMathew, S.Orazi, A.Lin, P.Wang, S. A.Bueso-Ramos, C. E.Foucar, K.Hasserjian, R. P.Hsi, E. D.
- [22] Complex Karyotype but Not Blast Percentage Is Associated with Poor Survival in Acute Myeloid Leukemia and Myelodysplastic Syndrome with Inv(3)(q21q26.2)/t(3;3)(q21;q26.2); a Bone Marrow Pathology Group StudyMODERN PATHOLOGY, 2013, 26 : 358A - 358ARogers, H. J.Vardiman, J. W.Anastasi, J.Raca, G.Savage, N. M.Cherry, A. M.Arber, D.Moore, E.Morrissette, J. J. D.Bagg, A.Liu, Y-CMathew, S.Orazi, A.Lin, P.Wang, S. A.Bueso-Ramos, C. E.Foucar, K.Hasserjian, R. P.Hsi, E. D.
- [23] Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2): Clinical and biological features and comparison with other acute myeloid leukemias with cytogenetic aberrations involving long arm of chromosome 3HEMATOLOGY, 2015, 20 (08) : 435 - 441Maria Raya, JoseMartin-Santos, TaidaLuno, ElisaSanzo, CarmenLuz Perez-Sirvent, MariaSuch, EsperanzaTomas Navarro, JoseMilla, FuensantaAlonso, EstherDomingo, AliciaRozman, MariaDiaz-Beva, MarinaBatlle, AnaGonzalez-de-Villambrosia, SoniaTuset, EsperanzaVallespi, TeresaOrtega, MargaritaBermejo, AlfredoMartin-Ramos, MarisaPeri, ValeriaSole, FrancescFlorensa, Lourdes
- [24] Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group studyHAEMATOLOGICA, 2014, 99 (05) : 821 - 829Rogers, Heesun J.Vardiman, James W.Anastasi, JohnRaca, GordanaSavage, Natasha M.Cherry, Athena M.Arber, DanielMoore, ErikaMorrissette, Jennifer J. D.Bagg, AdamLiu, Yen-ChunMathew, SusanOrazi, AttilioLin, PeiWang, Sa A.Bueso-Ramos, Carlos E.Foucar, KathrynHasserjian, Robert P.Tiu, Ramon V.Karafa, MatthewHsi, Eric D.
- [25] Clinical and Genomic Profiles of Korean Patients with MECOM Rearrangement and the t(3;21)(q26.2;q22.1) TranslocationANNALS OF LABORATORY MEDICINE, 2022, 42 (05) : 590 - +Lee, JikyoKim, Sung MinKim, SoonokYun, JiwonJeong, DajeongLee, Young EunRoh, Eun-YounLee, Dong Soon
- [26] Lenalidomide Plus Hypomethylating Agent for Acute Myeloid Leukemia (AML) with Recurrent Genetic Abnormalities -AML with Inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MecomBLOOD, 2018, 132Merz, Lauren E.Perissinotti, Anthony J.Marini, Bernard LawrenceCrouch, AshleyPettit, KristenBurke, Patrick W.Erba, Harry P.Bixby, Dale L.
- [27] Pediatric chronic myeloid leukemia with inv(3)(q21q26.2) and T lymphoblastic transformation: A case reportBiomarker Research, 4 (1)Lewen M.Gresh R.Queenan M.Paessler M.Pillai V.Hexner E.Frank D.Bagg A.Aplenc R.Caywood E.Wertheim G.
- [28] Acute myeloid leukemia with inv(3)(q21.3q26.2)/t(3;3)(q21.3;q26.2): Study of 61 patients treated with intensive protocolsEUROPEAN JOURNAL OF HAEMATOLOGY, 2020, 105 (02) : 138 - 147Sitges, MartaBoluda, BlancaGarrido, AnaMorgades, MireiaGranada, IsabelBarragan, EvaArnan, MontserratSerrano, JosefinaTormo, MarMiguel Bergua, JuanColorado, MercedesSalamero, OlgaEsteve, JordiBenavente, CelinaPerez-Encinas, ManuelColl, RosaMarti-Tutusaus, Josep-MariaBrunet, SalutSierra, Jorgeangel Sanz, MiguelMontesinos, PauRibera, Josep-MariaVives, Susana
- [29] Lenalidomide Plus Hypomethylating Agent as a Treatment Option in Acute Myeloid Leukemia With Recurrent Genetic Abnormalities-AML With inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOMCLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2020, 20 (01): : 24 - 30Merz, Lauren E.Perissinotti, Anthony J.Marini, Bernard L.Burke, Patrick W.Crouch, AshleyErba, Harry P.Bixby, Dale
- [30] The prognostic significance of an inv(3)(q21q26.2) in addition to a t(9;22)(q34;q11.2) in patients treated with tyrosine kinase inhibitorsCANCER GENETICS, 2014, 207 (05) : 171 - 176Theil, Karl S.Cotta, Claudiu V.