Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia [13]

2007-11-01

Leukemia , Volume 21 - Issue 11 p. 2382- 2384

Additional Metadata
Persistent URL	doi.org/10.1038/sj.leu.2404795, hdl.handle.net/1765/36242
Journal	Leukemia
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Wouters, B., Sanders, M., Lugthart, S., Geertsma-Kleinekoort, W., van Drunen, E., Beverloo, B., … Delwel, R. (2007). Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia [13]. Leukemia, 21(11), 2382–2384. doi:10.1038/sj.leu.2404795

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