APA (7th ed.) Citation

Allard, P., Tagliaferri, L., Weru, V., Cario, H., Lobitz, S., Grosse, R., . . . Eckert, M. (2024). The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β‐thalassaemia and no or low HbA expression. European Journal of Haematology, 113(4), 501. https://doi.org/10.1111/ejh.14259

Chicago Style (17th ed.) Citation

Allard, Pierre, et al. "The German Sickle Cell Disease Registry Reveals a Surprising Risk of Acute Splenic Sequestration and an Increased Transfusion Requirement in Patients with Compound Heterozygous Sickle Cell Disease HbS/β‐thalassaemia and No or Low HbA Expression." European Journal of Haematology 113, no. 4 (2024): 501. https://doi.org/10.1111/ejh.14259.

MLA (9th ed.) Citation

Allard, Pierre, et al. "The German Sickle Cell Disease Registry Reveals a Surprising Risk of Acute Splenic Sequestration and an Increased Transfusion Requirement in Patients with Compound Heterozygous Sickle Cell Disease HbS/β‐thalassaemia and No or Low HbA Expression." European Journal of Haematology, vol. 113, no. 4, 2024, p. 501, https://doi.org/10.1111/ejh.14259.