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

Item Type:	Article
Title:	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
Creators Name:	Hilgenfeld, E. and Padilla-Nash, H. and McNeil, N. and Knutsen, T. and Montagna, C. and Tchinda, J. and Horst, J. and Ludwig, W.D. and Serve, H. and Buechner, T. and Berdel, W.E. and Schroeck, E. and Ried, T.
Source:	British Journal of Haematology
ISSN:	0007-1048
Publisher:	Blackwell Publishing
Volume:	113
Page Range:	305-317
Date:	1 May 2001
PubMed:	View item in PubMed

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