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Hemoglobin|January 1, 1985
Hb F-Tokyo or alpha 2G gamma 2 34(B16)Val----Ile, a silent gamma chain variant detected by reverse phase high performance liquid chromatographyS Chen, J B Wilson, B B Webber, et al.Hemoglobin|July 17, 2020
Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian PopulationMohammad Hamid, Ebtesam Zargan Nezhad, Bijan Keikhaei, et al.Hemoglobin|March 26, 2015
Is the medical home for adult patients with sickle cell disease a reality or an illusion?Samir K Ballas, Elliott P VichinskyHemoglobin|April 10, 2015
First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese FamilyBiyan Chen, Peng Huang, Shang Yi, et al.Hemoglobin|July 11, 2020
Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular DiagnosisMing-Li Xu, Jia-Chun Qin, Bi-Yan Chen, et al.Hemoglobin|July 23, 2020
Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin GenesSalvador Payán-Pernía, Sara Bernal Noguera, Esther Rojas Rodríguez, et al.Hemoglobin|May 16, 2014
Screening and diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a prenatal control program for thalassemiaYu Yang, Ji-Wu Lou, Yan-Hui Liu, et al.Hemoglobin|May 16, 2014
α-Globin gene mutations in Isfahan Province, IranArezo Karamzade, Hadi Mirzapour, Majid Hoseinzade, et al.Hemoglobin|May 16, 2014
Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutationsRami A Jarjour, Hossam Murad, Faten Moasses, et al.Hemoglobin|January 1, 1985
Hemoglobin North Chicago (beta 36 [C2] proline----serine): a new high affinity hemoglobinS Rahbar, J Louis, T Lee, et al.Pageof 238