F. Speleman
Centre for Medical Genetics
Ghent University Hospital
Ghent
Belgium
Name/email consistency: high
- Copy number alterations and copy number variation in cancer: close encounters of the bad kind. Speleman, F., Kumps, C., Buysse, K., Poppe, B., Menten, B., De Preter, K. Cytogenet. Genome Res. (2008)
- A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias. Speleman, F., Cauwelier, B., Dastugue, N., Cools, J., Verhasselt, B., Poppe, B., Van Roy, N., Vandesompele, J., Graux, C., Uyttebroeck, A., Boogaerts, M., De Moerloose, B., Benoit, Y., Selleslag, D., Billiet, J., Robert, A., Huguet, F., Vandenberghe, P., De Paepe, A., Marynen, P., Hagemeijer, A. Leukemia (2005)