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-Reference-Cited by-同舟云学术

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

Published:2001-05 Issue:2 Volume:113 Page:305-317
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

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

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.02723.x/fullpdf

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4. Double Minutes and c-MYC amplification in acute myelogenous leukemia: are they prognostic factors?;Bruckert;Cancer Genetics and Cytogenetics,2000

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