Mendler, J. H., Maharry, K., Becker, H., Eisfeld, A.-K., Senter, L., Mrózek, K., … Bloomfield, C. D. (2013). In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline. Haematologica, 98(8), e92–e94. https://doi.org/10.3324/haematol.2013.089904

Mendler, Jason H., Kati Maharry, Heiko Becker, Ann-Kathrin Eisfeld, Leigha Senter, Krzysztof Mrózek, Jessica Kohlschmidt, et al. “In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline.” Haematologica 98, no. 8 (August 2013): e92–94. https://doi.org/10.3324/haematol.2013.089904.

Mendler JH, Maharry K, Becker H, Eisfeld A-K, Senter L, Mrózek K, et al. In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline. Haematologica. 2013 Aug;98(8):e92–4.

Mendler, Jason H., et al. “In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline.” Haematologica, vol. 98, no. 8, Aug. 2013, pp. e92–94. Pubmed, doi:10.3324/haematol.2013.089904.

Mendler JH, Maharry K, Becker H, Eisfeld A-K, Senter L, Mrózek K, Kohlschmidt J, Metzeler KH, Schwind S, Whitman SP, Khalife J, Caligiuri MA, Klisovic RB, Moore JO, Carter TH, Marcucci G, Bloomfield CD. In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline. Haematologica. 2013 Aug;98(8):e92–e94.