[1. Dickinson HO. The causes of childhood leukaemia. BMJ. 2005; 330: 1279-1280.]Search in Google Scholar
[2. Rowley JD, Le Beau MM, Rabbitts TH. Chromosomal translocations and genome rearrangements in cancer. Cham: Springer 2015.]Search in Google Scholar
[3. Golub TR, Barker GF, Bohlander SK, et al. Fusionof the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc Nat Acad Sci U S A. 1995; 92: 4917-4921.]Search in Google Scholar
[4. Romana SP, Mauchauff e M, Le Coniat M, et al. The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood. 1995; 85: 3662-3670.]Search in Google Scholar
[5. Geyer MB, Hsu M, Devlin SM, et al. Overall survival among older US adults with ALL remains low despite modest improvement since 1980: SEER analysis. Blood. 2017; 129: 1878-81.]Search in Google Scholar
[6. Clarke RT, Van den Bruel A, Bankhead C, et al. Clinical presentation of childhood leukaemia: a systematic review and meta-analysis. Arch Dis Child. 2016; 101(10): 894-901.]Search in Google Scholar
[7. Horibe K, Saito AM, Takimoto T et al. Incidence and survival rates of hematological malignancies in Japanese children and adolescents (2006-2010): Based on registry data from the Japanese Society of Pediatric Hematology. Int J Hematol. 2013; 98: 74-88.]Search in Google Scholar
[8. Inaba H, Mullighan CG. Pediatric acute lymphoblastic leukemia. Haematologica. 2020; 105(11): 2524-2539.]Search in Google Scholar
[9. Pui CH, Yang JJ, Hunger SP, et al. Childhood Acute Lymphoblastic Leukemia: Progress Through Collaboration. J Clin Oncol. 2015; 33(27): 2938-48.]Search in Google Scholar
[10. Van Dongen JJ, Macintyre EA, Gabert JA, et al. Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual disease. Report of the BIOMED-1 Concerted Action: investigation of minimal residual disease in acute leukemia. Leukemia. 1999; 13(12): 1901-28.]Search in Google Scholar
[11. Seeger K, Buchwald D, Peter A, et al. TEL-AML1 fusion in relapsed childhood acute lymphoblastic leukemia. Blood. 1999; 94(1): 374-376.]Search in Google Scholar
[12. Li X, Sundquist K, Sundquist J et al. Family history of early onset acute lymphoblastic leukemia is suggesting genetic associations. Sci Rep. 2021; 11(1): 12370.]Search in Google Scholar
[13. Holmfeldt L, Wei L, Diaz-Flores E, et al. The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nat Genet. 2013; 45(3): 242-252.]Search in Google Scholar
[14. Moriyama T, Metzger ML, Wu G, et al. Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study. Lancet Oncol. 2015; 16(16): 1659-1666.]Search in Google Scholar
[15. Shah S, Schrader KA, Waanders E, et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nat Genet. 2013; 45(10): 1226-1231.]Search in Google Scholar
[16. Noetzli L, Lo RW, Lee-Sherick AB, et al. Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia. Nat Genet. 2015; 47(5): 535-538.]Search in Google Scholar