Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance

MLA

M. Hein, et al. “Comprehensive Array CGH of Normal Karyotype Myelodysplastic Syndromes Reveals Hidden Recurrent and Individual Genomic Copy Number Alterations with Prognostic Relevance.” Leukemia, vol. 25, Jan. 2011, pp. 387–99. EBSCOhost, https://doi.org/10.1038/leu.2010.293.

APA

M. Hein, Anne Thiel, C Evers, D. Ingenhag, Barbara Hildebrandt, Manfred Beier, K. Servan, Beate Betz, Ulrich Germing, Brigitte Royer-Pokora, & V Moeller. (2011). Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance. Leukemia, 25, 387–399. https://doi.org/10.1038/leu.2010.293

Chicago

M. Hein, Anne Thiel, C Evers, D. Ingenhag, Barbara Hildebrandt, Manfred Beier, K. Servan, et al. 2011. “Comprehensive Array CGH of Normal Karyotype Myelodysplastic Syndromes Reveals Hidden Recurrent and Individual Genomic Copy Number Alterations with Prognostic Relevance.” Leukemia 25 (January): 387–99. doi:10.1038/leu.2010.293.