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Hemoglobin|January 1, 1982
Synthesis of hemoglobin chains in adult and newborn goats: possible influence of the beta c synthesis on the production of alpha chainsE C Abraham, M Stallings, T H HuismanHemoglobin|January 1, 1982
Interaction of chromosomes bearing 1, 2 or 3 alpha-globin genes in an American black family with alpha-thalassemiaG B Sancar, M M Cedeno, R Bellevue, et al.Hemoglobin|January 1, 1981
Hemoglobin Tottori (alpha 59[E8] glycine replaced by valine)T Nakatsuji, S Miwa, Y Ohba, et al.Hemoglobin|January 1, 1978
Measuring relative electrophoretic mobilities of mutant hemoglobins and globin chainsR G Schneider, R C BarwickHemoglobin|January 1, 1981
Molecular stability of Hb Philly (alpha 2 beta 2 35(Cl) Tyr leads to Phe). Rhe relationship of hemoglobin stability to ligand state as defined by heat and mechanical shaking testsT Asakura, K Adachi, E Schwartz, et al.Hemoglobin|January 1, 1977
Modification of the acid elution technique for quantitation of fetal hemoglobin in individual erythrocytesS C Bernstein, J E Bowman, H H SwiftHemoglobin|January 1, 1982
Soluble and stroma-bound globin chains in mild and severe beta thalassemiaA S Braverman, L Schwartzberg, R BerkowitzHemoglobin|June 27, 2015
Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia IntermediaMehran Karimi, Nargess Arandi, Sezaneh Haghpanah, et al.Hemoglobin|July 11, 2015
The Molecular Basis of α-Thalassemia in the Qatari Pediatric PopulationMadeeha Kamal, Shaza Abu-Sirriya, Aseel Abu-Dayya, et al.Hemoglobin|July 17, 2015
First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese PatientSheng He, Qiang Zhang, Chenguang Zheng, et al.Pageof 240