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Hemoglobin|January 10, 2018
The Assessment and Sustainable Management of Sickle Cell Disease in the Indigenous Tharu Population of NepalMiles Marchand, Carson Gill, Armaan K Malhotra, et al.Hemoglobin|January 10, 2018
Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) VariantAparna A Bhanushali, Kumari Himani, Pradeep K Patra, et al.Hemoglobin|January 10, 2018
A Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in BangladeshAbdul Aziz, Sudipta A Das, Waqar A Khan, et al.Hemoglobin|November 11, 2017
Prenatal Diagnosis and Molecular Analysis of a Large Novel Deletion (- -JS) Causing α0-ThalassemiaJinru Cao, Shuzhen He, Yudong Pu, et al.Hemoglobin|January 11, 2019
A Rapid, Affordable and Feasible Method for Detection of the HBG1: g.-225_-222delAGCA PolymorphismMarco Musso, Gian Luca ForniHemoglobin|January 1, 1991
Hb A2-Parkville or delta 47(CD6)Asp----Val, a new delta chain variantH Leung, A T Gilbert, P J Fleming, et al.Hemoglobin|January 1, 1991
Polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 (6Val) (Hb S) and alpha 2 beta 2(6Leu) (Hb Leu)K Adachi, E Rappaport, H S Eck, et al.Hemoglobin|January 1, 1991
Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variantsR B Gupta, R S Tiwary, P L Pande, et al.Hemoglobin|April 18, 2009
Two new examples of Hb St. Etienne [beta 92(F8)HisGln] in association with venous thrombosisNicholas H C Au, Ann Y K Wong, Linda Vickars, et al.Hemoglobin|April 18, 2009
beta-Thalassemia mutations in the Iranian Kurdish population of Kurdistan and West Azerbaijan provincesMehdi Haghi, Shohre Khorshidi, Mohammad Ali Hosseinpour Feizi, et al.Pageof 239