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pro vyhledávání: '"Bahra K Hamad"'
Autor:
Sarkar S Aziz, Bahra K Hamad, Hero O Hamad, Muzhda I Qader, Eman N Ali, Rayan H Muhammed, Mudhir Sabir Shekha
Publikováno v:
Iraqi Journal of Hematology, Vol 11, Iss 1, Pp 19-24 (2022)
BACKGROUND: Thalassemia syndromes and structural hemoglobin variants generate blood crisis of variable clinical symptoms, ranging from mild-to-moderate hematological disorder to severe, lifelong, transfusion-dependent anemia. The aim of current study
Externí odkaz:
https://doaj.org/article/d23f7d758a514acfa3a2a0f408cd3440
