Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Firouzjahi AR (MD)"'
Autor:
Akhavan-Niaki H (PhD), Pourtaghi M (MD), Firouzjahi AR (MD), Banihashemi A (BSc), Sedaghat S (MD)
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 14, Iss 1, Pp 75-82 (2012)
Background and Objective: Alpha thalassemia is one of the most common hemoglobin disorders. Some combination of alpha globin gene mutations may cause HbH disease with severe anemia or intermediate thalassemia. genotype common deletions are routinely
Externí odkaz:
https://doaj.org/article/6fdb37a9c09f44a8abe626e36228a105
