Motovali-Bashi, M., & Ghasemi, T. (2015). Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients. Iran Biomed J.
Styl ChicagoMotovali-Bashi, Majid, a Tayyebeh Ghasemi. "Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level At Isfahanian Intermediate β-Thalassemia Patients." Iran Biomed J 2015.
Citace podle MLAMotovali-Bashi, Majid, a Tayyebeh Ghasemi. "Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level At Isfahanian Intermediate β-Thalassemia Patients." Iran Biomed J 2015.
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