APA Citation

Campregher, P. V., Helman, R., Pereira, W. O., Puga, R. D., Lisboa, B., Ascendino, E. H., . . . De Souza Santos, F. P. (2014). The presence of ASXL1 mutations as well as a total number of myeloid driver mutations higher than two is strongly associated with the diagnosis of primary myelofibrosis as opposed to essential thrombocythemia.

Chicago Style Citation

Campregher, Paulo Vidal, et al. The Presence of ASXL1 Mutations As Well As a Total Number of Myeloid Driver Mutations Higher Than Two Is Strongly Associated With the Diagnosis of Primary Myelofibrosis As Opposed to Essential Thrombocythemia. 2014.

MLA Citation

Campregher, Paulo Vidal, et al. The Presence of ASXL1 Mutations As Well As a Total Number of Myeloid Driver Mutations Higher Than Two Is Strongly Associated With the Diagnosis of Primary Myelofibrosis As Opposed to Essential Thrombocythemia. 2014.

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