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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

F. Speleman

Centre for Medical Genetics

Ghent University Hospital

Ghent

Belgium

[email]@ugent.be

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium. 2005 - 2008

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
 
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