1. Choi HJ, Kim HR, Shin MG, et al. 2011; Spectra of chromosomal aberrations in 325 leukemia patients and implications for the development of new molecular detection systems. J Korean Med Sci. 26:886–92. DOI:
10.3346/jkms.2011.26.7.886. PMID:
21738341. PMCID:
PMC3124718.
Article
2. Bacher U, Kern W, Schnittger S, Hiddemann W, Schoch C, Haferlach T. 2005; Further correlations of morphology according to FAB and WHO classification to cytogenetics in de novo acute myeloid leukemia: a study on 2,235 patients. Ann Hematol. 84:785–91. DOI:
10.1007/s00277-005-1099-0. PMID:
16132906.
Article
3. Klaus M, Haferlach T, Schnittger S, Kern W, Hiddemann W, Schoch C. 2004; Cytogenetic profile in de novo acute myeloid leukemia with FAB subtypes M0, M1, and M2: a study based on 652 cases analyzed with morphology, cytogenetics, and fluorescence in situ hybridization. Cancer Genet Cytogenet. 155:47–56. DOI:
10.1016/j.cancergencyto.2004.03.008. PMID:
15527902.
Article
4. Betts DR, Ammann RA, Hirt A, et al. 2007; The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG). Eur J Haematol. 78:468–76. DOI:
10.1111/j.1600-0609.2007.00854.x. PMID:
17419750.
Article
5. Nakase K, Bradstock K, Sartor M, et al. 2000; Geographic heterogeneity of cellular characteristics of acute myeloid leukemia: a comparative study of Australian and Japanese adult cases. Leukemia. 14:163–8. DOI:
10.1038/sj.leu.2401638. PMID:
10637492.
Article
6. Cheng Y, Wang Y, Wang H, et al. 2009; Cytogenetic profile of de novo acute myeloid leukemia: a study based on 1432 patients in a single institution of China. Leukemia. 23:1801–6. DOI:
10.1038/leu.2009.107. PMID:
19474801.
Article
7. Xie Y, Davies SM, Xiang Y, Robison LL, Ross JA. 2003; Trends in leukemia incidence and survival in the United States (1973-1998). Cancer. 97:2229–35. DOI:
10.1002/cncr.11316. PMID:
12712476.
Article
8. Irigaray P, Newby JA, Clapp R, et al. 2007; Lifestyle-related factors and environmental agents causing cancer: an overview. Biomed Pharmacother. 61:640–58. DOI:
10.1016/j.biopha.2007.10.006. PMID:
18055160.
Article
9. Pallisgaard N, Hokland P, Riishøj DC, Pedersen B, Jørgensen P. 1998; Multiplex reverse transcription-polymerase chain reaction for simultaneous screening of 29 translocations and chromosomal aberrations in acute leukemia. Blood. 92:574–88. DOI:
10.1182/blood.V92.2.574. PMID:
9657758.
Article
10. Hutchings Hoffmann M, Wirenfeldt Klausen T, Hasle H, Schmiegelow K, Brondum-Nielsen K, Johnsen HE. 2005; Multiplex reverse transcription polymerase chain reaction screening in acute myeloid leukemia detects cytogenetically unrevealed abnormalities of prognostic significance. Haematologica. 90:984–6. PMID:
15996940.
11. Strehl S, König M, Mann G, Haas OA. 2001; Multiplex reverse transcriptase-polymerase chain reaction screening in childhood acute myeloblastic leukemia. Blood. 97:805–8. DOI:
10.1182/blood.V97.3.805. PMID:
11157501.
Article
12. Elia L, Mancini M, Moleti L, et al. 2003; A multiplex reverse transcriptase-polymerase chain reaction strategy for the diagnostic molecular screening of chimeric genes: a clinical evaluation on 170 patients with acute lymphoblastic leukemia. Haematologica. 88:275–9. PMID:
12651265.
15. Pullarkat V, Slovak ML, Kopecky KJ, Forman SJ, Appelbaum FR. 2008; Impact of cytogenetics on the outcome of adult acute lymphoblastic leukemia: results of Southwest Oncology Group 9400 study. Blood. 111:2563–72. DOI:
10.1182/blood-2007-10-116186. PMID:
18156492. PMCID:
PMC2254550.
Article
16. Amare P, Gladstone B, Varghese C, Pai S, Advani S. 1999; Clinical significance of cytogenetic findings at diagnosis and in remission in childhood and adult acute lymphoblastic leukemia: experience from India. Cancer Genet Cytogenet. 110:44–53. DOI:
10.1016/S0165-4608(98)00179-4. PMID:
10198622.
17. Chang HH, Lu MY, Jou ST, Lin KH, Tien HF, Lin DT. 2006; Cytogenetics in childhood acute lymphoblastic leukemia in Taiwan: a single- institutional experience. Pediatr Hematol Oncol. 23:495–506. DOI:
10.1080/08880010600739368. PMID:
16849281.
19. Kim MH, Hwang HY, Jeong SH, et al. 2000; Detection of p53 mutant and isochromosome 17q in myelodysplastic syndromes and leukemias. Korean J Clin Pathol. 20:349–53.