Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart's disease: A hematological, molecular, and diagnostic aspects.

MLA

Singha, Kritsada, et al. “Severe Thalassemia Syndrome Caused by Hemoglobin Pak Num Po AEBart’s Disease: A Hematological, Molecular, and Diagnostic Aspects.” International Journal of Laboratory Hematology, vol. 42, no. 4, Aug. 2020, pp. e173–76. EBSCOhost, https://doi.org/10.1111/ijlh.13224.

APA

Singha, K., Wiangnon, S., Fucharoen, G., Jetsrisuparb, A., Komwilaisak, P., & Fucharoen, S. (2020). Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects. International Journal of Laboratory Hematology, 42(4), e173–e176. https://doi.org/10.1111/ijlh.13224

Chicago

Singha, Kritsada, Surapon Wiangnon, Goonnapa Fucharoen, Arunee Jetsrisuparb, Patcharee Komwilaisak, and Supan Fucharoen. 2020. “Severe Thalassemia Syndrome Caused by Hemoglobin Pak Num Po AEBart’s Disease: A Hematological, Molecular, and Diagnostic Aspects.” International Journal of Laboratory Hematology 42 (4): e173–76. doi:10.1111/ijlh.13224.