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Hemoglobin|December 17, 2009
Osteopenia-osteoporosis syndrome in patients with thalassemia: understanding of type of bone disease and response to treatmentRatna Chatterjee, Rekha BajoriaHemoglobin|December 17, 2009
Heart disease in thalassemia intermediaA Aessopos, M Tsironi, A Andreopoulos, et al.Hemoglobin|December 17, 2009
Allogeneic stem cell transplantation in patients with β-thalassemia: King Faisal specialist hospital and research centre experienceA Al-Jefri, A Ayas, A Al Musa, et al.Hemoglobin|December 17, 2009
Blood transfusion: quality and safety issues in thalassemia, basic requirements and new trendsJohn PorterHemoglobin|December 5, 2009
A novel polymorphism causes a different restriction pattern by RsaI in the beta-globin gene cluster: application in prenatal diagnosisAtefeh Valaei, Fatemeh Bayat, Alireza Kordafshari, et al.Hemoglobin|December 5, 2009
Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian familiesIndu Voruganti, Barry Eng, John S WayeHemoglobin|December 5, 2009
Molecular analysis of gamma-globin promoters, HS-111 and 3'HS1, in beta-thalassemia intermedia patients associated with high levels of Hb FMohammad Hamid, Frouzandeh Mahjoubi, Mohammad T Akbari, et al.Hemoglobin|December 5, 2009
alpha-Thalassemia caused by two novel splice mutations of the alpha2-globin gene: IVS-I-1 (G>A and G>T)John S Waye, Barry Eng, Fabrizio Dutly, et al.Pageof 238