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pro vyhledávání: '"Mohammed Abdalgayoom"'
Autor:
Khaled Ferih, Basel Elsayed, Amgad M. Elshoeibi, Ahmed A. Elsabagh, Mohamed Elhadary, Ashraf Soliman, Mohammed Abdalgayoom, Mohamed Yassin
Publikováno v:
Diagnostics, Vol 13, Iss 9, p 1551 (2023)
Thalassemia is an autosomal recessive genetic disorder that affects the beta or alpha subunits of the hemoglobin structure. Thalassemia is classified as a hypochromic microcytic anemia and a definitive diagnosis of thalassemia is made by genetic test
Externí odkaz:
https://doaj.org/article/20acc47353054f9cb5221a2f013213ff