References
1. Hastings R, Howell R, Betts D, Porter S, Haferlach C, Dastugue N, Radford-Weiss I, Beverloo H, Simons A, Mellink C, Snijder S, Ruiter E, Schoumans J, Espinet B, Siebert R, Couturier J, Bernheim A, Solé F, Luquet I, Stioui S, Cavani S. Guidelines and Quality Assurance for Acquired Cytogenetics A common Euro-pean framework for quality assessment for banded chromosome studies and molecular cytogenetic investigations of acquired abnormalities. European Cytogenetics Association Newsletter. 2013;No 13.
2. Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM, Bloomfield CD, Cazzola M, Vardiman JW. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016;127:2391-2405.
3. Chotirat S, Thongnoppakhun W, Promsuwicha O, Boonthimat C and Auewarakul C. Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients. Journal of Hematology and Oncology. 2012; 5: 5.
4. Eleni LD, Nicholas ZC, Alexandros S. Challenges in treating older patients with acute myeloid leukemia. Journal of oncology. 2010;2010: 823-943
5. Thol F, Schlenk RF, Heuser M, Ganser A. How I treat refractory and early relapsed acute myeloid leukemia. Blood. 2015; 26(3): 319–327.
6. Campbell L. Cytogenetic and FISH techniques in myeloid malignancies. Methods Mol Med. 2006; 125: 13-28.
7. Dohner H, Estey EH, AmadoriS, Appelbaum FR, Buhner T, Burnett A, Dombret H, Fenaux P, Grimwade D, Larson RA, Lo-Coco F, Naoe T, Niederwieser D, Ossenkoppele GJ, Sanz MA, Sierra J, Tallman MS, Lo Wenberg B, Bloomfield CD. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European Leukemia Net. Blood. 2010; 115: 453-474.
8. O’Donnell MR, Tallman MS, Abboud CN, Altman JK, Appelbaum FR, Arber DA, Altar E, et al. Acute myeloid leukemia: NCCN clinical practice guidelines in oncology. National Comprehensive Cancer Network On- Line. 2014; 2
9. Baer M and Greer J. In Acute myeloid leukemia in adults. In: Wintrobe‘s clinical hematology. Greer JP, Arber DA, Glader B, List Af, Jr RTM, Paraskevas F, Rodgers GM and Foester J (eds.), (13th edition), Lippincott Williams and Wilkins, Wolters Kluwer Health, Philadelphia, USA. 2009; Chapter 79: 1843-1846.
10. Sole F, Florensa L, Espinet B, Basses C, Lioveras E and Woessner S. Absence of BCR/ABL rearrangement in 41 patients with essential thrompocytopenia. Haematologica. 2000; 85: 214-215.
11. Breems D, Van Putten W, Georgine E, Greef D, Shama L, Bhola V, Klasien B, Schoorl G, Clemens H, Mellink, Nieuwint A, Jotterand M, Hagemeijer A, Beverloo H, and Lowenberg B. Monosomal Karyotype in Acute Myeloid Leukemia: A Better Indicator of Poor Prognosis Than a Complex Karyotype. Journal of Clinical Oncology. 2008; 26: 4791-4797.
12. Hamad N, Elconin J, Karnoub A, Bai W, Rich J, Abraham R, Der C. Distinct requirements for Ras oncogenesis in human versus mouse cells. Genes & Dev. 2002; 16: 2045-57.
13. Fasan A, Haferlach C, Alpermann T, Kern W, Haferlach T and Schnittger S. A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98-NSD1 fusion gene. Leukemia. 2013; 27: 245-248.
14. Heim S and Mittelman F. Acute myeloid leukemia. Cancer Cytogenetics. 1995; 2nd ed. New York: Willey-Liss: 69-140.
15. Döhner K and Döhner H. Molecular characterization of acute myeloid leukemia. Haematologica. 2008; 93: 976-982.
16. Bryan L and Jay L. Acute Myeloid Leukemia Diagnosis in the 21st Century. Arch Pathol Lab Med. 2010; 134: 1427–1433.
17. Kim S, Kim D, Jang J, Jung C and Jang M. Novel mutations in CEBPA in Korean Patients with acute myeloid leukemia with a normal karyotype. Ann Lab Med. 2012; 32: 153-157.
18. Kayser S, Zucknick M, Döhner K, Krauter J, Köhne C, Horst H, Held G, T-Toal, Wilhelm S, Rummel T, Germing U, Götze K, Nachbaur D, Schlegelberger B, Göhring G, Späth D, Morlok C, Teleanu V, Ganser A, Döhner H, Schlenk R, and for the German-Austrian AML Study Group. Monosomal karyotype in adult acute myeloid leukemia: prognostic impact and outcome after different treatment strategies. Blood. 2012; 119: 551-558.
19. Shimada A, Taki T, Tabuchi K, Tawa A, Horibe K, Tsuchida M, Hanada R, Tsukimoto I, and Hayashi Y. KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t (8; 21): a study of the Japanese Childhood AML Cooperative Study Group. Blood. 2006; 107: 1806-1809.
20. Evans J, Czepulkowski B, Gibbons B, Swansbury G and Chessells J. Childhood monosomy 7 revisited. Br J Haematol.1988; 69: 41-5.
21. Warner JK, Wang JY, Hope KJ, Jin L and Dick JE. Concepts of human leukemic development. Oncogene. 2004; 23: 7164–7177.
22. Wolman S, Gundacker H, Appelbaum F, and Slovak M. Impact of trisomy 8 on clinical presentation, treatment response and survival in acute myeloid leukemia: a Southwest Oncology Group study. Blood. 2002; 100: 29-35.
23. Bakshi S, Brahmbhatt M, Trivedi P, Dalal E, Patel D, Purani S, Shukla S, Shah P and Patel P. Trisomy 8 in leukemia; A GCRI experience. Indian Journal of Human Genetics. 2012; 18: 106-108.
24. Elliott M, Letendre L, Tefferi A, Hanson C and Dewald G. Trisomy 8 in acute myeloid leukemia (AML). Blood. 2000; 96: 708.
25. Schoch C, Haase D, Fonatsch C, Haferlach T, Löffler H, Schlegelberger B, Hossfeld D, Becher R, Sauerland M, Heinecke A, Wörmann B, Büchner T, Hiddemann W and for the German AML Cooperative Study Group. The significance of trisomy 8 in de novo acute myeloid leukaemia: the accompanying chromosome aberrations determine the prognosis. British Journal of Haematology. 1997; 99: 605-611.
26. Paulsson K, Lassen C, Kuric N, Billstrom R, Fioretos T, Tanke H and Johansson B. MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes. Leukemia. 2003; 17: 813-816.
27. McKinney C, Golden W, Gemma N, Swerdlow S and Williams M. RARA and PML gene rearrangements in acute promyelocytic leukemia with complex translocations and atypical features. Genes Chromosomes Cancer. 1994; 9: 49-56.
28. Sucić M, Zadro R, Burazer B, Labar B, Nemet D, Mrsić M, Aurer I, Mrsić S, Hitrec V, Boban D, Glamocak M, Batinić D, Uzarević B and Rukavina A. Acute promyelocytic leukemia M3: cytomorph-ologic, immunophenotypic, cytogenetic, and molecular variants. J Hematother Stem Cell Res. 2002; 11(6): 941-50.
29. Grimwade D and Solomon E. Characterisation of the PML/RAR alpha rearrangement associated with t (15; 17) acute promyelocytic leukaemia. Curr Top Microbiol Immunol. 1997; 220: 81-112.
30. Chen Y, Kantarjian H, Pierce S, Faderl S, O’Brien S, Qiao W, Abruzzo L, De Lima M, Kebriaei P, Jabbour E, Daver N, Kadia T, Estrov Z, Garcia-Manero G, Cortes J and Ravandi F. Prognostic significance of 11q23 aberrations in adult acute myeloid leukemia and the role of allogeneic stem cell transpla-ntation. Leukemia. 2013; 27: 836-842.
31. Chauffaille M, Figueiredo M, Beltrani R, Antunes S, Yamamoto M and Kerbauy J. Acute promyelocytic leukemia: the study of t (15; 17) translocation by fluorescent in situ hybridization, reverse transcriptase-polymerase chain reaction and cytogenetic techniques. Research. 2001; 34: 735-743.
32. Yuan Y, Zhou L, Miyamoto T, Iwasaki H, Christopher J, Sebastien A, Burel, Lagasse E, Weissman I, Akashiffi K, and Zhang D. AML1-ETO expression is directly involved in the development of acute myeloid leukemia in the presence of additional mutations. Proc Natl Acad Sci U S A. 2001; 98(18): 10398–10403.
33. Lowenberg B, Downing J and Burnett A. Acute Myeloid Leukemia. The New English Journal of Medicine. 1999; 341: 1051-1062.
34. Shurtleff SA, Meyers S, Hiebert SW, Raimondi SC, Head DR, Willman CL, Wolman S, Slovak ML,Carroll AJ, Behm F, Hulshof MG, Motroni TA, Okuda T, Liu P, Collins FS, Downing JR. Heterogeneity in CBFb/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia. Blood. 1995; 85: 3695.
35. Raidmondi S and Heermema N. In Cytogenetics in children, adolescents and young adults; in ALL and AML. In Hematological Malignancies in Children, Adolescents and Young Adults, (first edition), Cairo MS and Sherrie L Perkins (eds.). 2012; Chapter 5: 101-120., Singapore; World Scientific.
36. Gröschel S, Sanders MA, Hoogenboezem R, et al. Mutational spectrum of myeloid malignancies with inv(3)/t(3;3) reveals a predominant involvement of RAS/RTK signaling pathways. Blood. 2015; .