Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2

E. Hilgenfeld, H. Padilla-Nash, N. McNeil, T. Knutsen, C. Montagna, J. Tchinda, J. Horst, W. D. Ludwig, H. Serve, T. Büchner, W. E. Berdel, E. Schröck, T. Ried

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