Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder.

MLA

Prieto-Conde, María Isabel, et al. “Genomic Analysis of a Familial Myelodysplasia/Acute Myeloid Leukemia and Inherited RUNX1 Mutations without a Pre-Existing Platelet Disorder.” Leukemia & Lymphoma, vol. 61, no. 1, Jan. 2020, pp. 181–84. EBSCOhost, https://doi.org/10.1080/10428194.2019.1648801.

APA

Prieto-Conde, M. I., Labrador, J., Hermida, G., Alonso, S., Jiménez, C., García-Álvarez, M., Medina, A., Balanzategui, A., Alcoceba, M., Sarasquete, M. E., Puig, N., González, V., Gutiérrez, N. C., García-Sanz, R., González-Díaz, M., & Chillón, M. del C. (2020). Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder. Leukemia & Lymphoma, 61(1), 181–184. https://doi.org/10.1080/10428194.2019.1648801

Chicago

Prieto-Conde, María Isabel, Jorge Labrador, Gerardo Hermida, Sara Alonso, Cristina Jiménez, María García-Álvarez, Alejandro Medina, et al. 2020. “Genomic Analysis of a Familial Myelodysplasia/Acute Myeloid Leukemia and Inherited RUNX1 Mutations without a Pre-Existing Platelet Disorder.” Leukemia & Lymphoma 61 (1): 181–84. doi:10.1080/10428194.2019.1648801.