Cite
Paroxysmal nocturnal hemoglobinuria clones are not infrequent in patients with inherited bone marrow failure syndromes.
MLA
Sreedharanunni, Sreejesh, et al. “Paroxysmal Nocturnal Hemoglobinuria Clones Are Not Infrequent in Patients with Inherited Bone Marrow Failure Syndromes.” European Journal of Haematology, vol. 99, no. 2, Aug. 2017, pp. 194–95. EBSCOhost, https://doi.org/10.1111/ejh.12898.
APA
Sreedharanunni, S., Varma, N., Sachdeva, M. U. S., Naseem, S., Malhotra, P., Bansal, D., Sood, A., Bose, P., & Varma, S. (2017). Paroxysmal nocturnal hemoglobinuria clones are not infrequent in patients with inherited bone marrow failure syndromes. European Journal of Haematology, 99(2), 194–195. https://doi.org/10.1111/ejh.12898
Chicago
Sreedharanunni, Sreejesh, Neelam Varma, Man Updesh Singh Sachdeva, Shano Naseem, Pankaj Malhotra, Deepak Bansal, Anil Sood, Parveen Bose, and Subhash Varma. 2017. “Paroxysmal Nocturnal Hemoglobinuria Clones Are Not Infrequent in Patients with Inherited Bone Marrow Failure Syndromes.” European Journal of Haematology 99 (2): 194–95. doi:10.1111/ejh.12898.