Cita APA

Mwesigwa, S., Moulds, J. M., Chen, A., Flanagan, J., Sheehan, V. A., George, A., & Hanchard, N. A. (2017). Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition. Transfusion.

Chicago Style Citation

Mwesigwa, Savannah, Joann M. Moulds, Alice Chen, Jonathan Flanagan, Vivien A. Sheehan, Alex George, i Neil A. Hanchard. "Whole-exome Sequencing of Sickle Cell Disease Patients With Hyperhemolysis Syndrome Suggests a Role for Rare Variation in Disease Predisposition." Transfusion 2017.

Cita MLA

Mwesigwa, Savannah, et al. "Whole-exome Sequencing of Sickle Cell Disease Patients With Hyperhemolysis Syndrome Suggests a Role for Rare Variation in Disease Predisposition." Transfusion 2017.