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References
Mitelman F . The cytogenetic scenario of chronic myeloid leukemia Leuk Lymphoma 1993 11: 11–15
Sessarego M, Fugazza G, Bruzzone R, Patrone F . Variant Philadelphia chromosome translocations are frequently associated with additional structural abnormalities Cancer Genet Cytogenet 1994 73: 57–59
Dewald GW, Wyatt WA, Juneau AL, Carlson RO, Zinsmeister AR, Jalal SM, Spurbeck JL, Silver RT . Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia Blood 1998 91: 3357–3365
Schrock E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Ried T . Multicolor spectral karyotyping of human chromosomes Science 1996 273: 494–497
Lemaire V, Jamar M, Evrard A, Augonbron V, Verheyen V, Koulischer L, Herens C . Deletions of 9q proximal to the ABL gene in standard and variant Philadelphia translocations: a new recurrent anomaly observed in more than 10% of CML patients Cytogenet Cell Genet 1999 85: 77
Grand F, Kulkarni S, Chase A, Goldman JM, Gordon M, Cross NC . Frequent deletion of hSNF5/INI1, a component of the SWI/SNF complex, in chronic myeloid leukemia Cancer Res 1999 59: 3870–3874
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Markovic, V., Bouman, D., Bayani, J. et al. Lack of BCR/ABL reciprocal fusion in variant Philadelphia chromosome translocations: a use of double fusion signal FISH and spectral karyotyping. Leukemia 14, 1157–1160 (2000). https://doi.org/10.1038/sj.leu.2401718
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DOI: https://doi.org/10.1038/sj.leu.2401718
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