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pro vyhledávání: '"Ketaki Prashant Mannur"'
Publikováno v:
Global Journal of Transfusion Medicine, Vol 8, Iss 1, Pp 92-95 (2023)
Thalassemia syndromes represent a group of inherited disorders characterized by decreased synthesis of one or more of the four globin chains in hemoglobin. The clinical spectrum ranges from asymptomatic carrier state to transfusion-dependent severe d
Externí odkaz:
https://doaj.org/article/ce13a2e42ce54613884fc30e9e271e75
