APA (7th ed.) Citation

Meggendorfer, M., Bacher, U., Alpermann, T., Haferlach, C., Kern, W., Gambacorti-Passerini, C., . . . Schnittger, S. (2013). SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations. Leukemia (08876924), 27(9), 1852. https://doi.org/10.1038/leu.2013.133

Chicago Style (17th ed.) Citation

Meggendorfer, M., U. Bacher, T. Alpermann, C. Haferlach, W. Kern, C. Gambacorti-Passerini, T. Haferlach, and S. Schnittger. "SETBP1 Mutations Occur in 9% of MDS/MPN and in 4% of MPN Cases and Are Strongly Associated with Atypical CML, Monosomy 7, Isochromosome I(17)(q10), ASXL1 and CBL Mutations." Leukemia (08876924) 27, no. 9 (2013): 1852. https://doi.org/10.1038/leu.2013.133.

MLA (9th ed.) Citation

Meggendorfer, M., et al. "SETBP1 Mutations Occur in 9% of MDS/MPN and in 4% of MPN Cases and Are Strongly Associated with Atypical CML, Monosomy 7, Isochromosome I(17)(q10), ASXL1 and CBL Mutations." Leukemia (08876924), vol. 27, no. 9, 2013, p. 1852, https://doi.org/10.1038/leu.2013.133.