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Hemoglobin|October 24, 2012
Study of serum hepcidin in hereditary hemolytic anemiasAmal El Beshlawy, Ibrahim Alaraby, Mohamed S E M Abdel Kader, et al.Hemoglobin|January 18, 2014
Hb Grand Junction (HBB: c.348_349delinsG; p.His117IlefsX42): a new hyperunstable hemoglobin variantMichael W Kent, Jennifer L Oliveira, James D Hoyer, et al.Hemoglobin|May 1, 2023
Effect of α+ Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based StudyPrasanta Purohit, Pradeep Kumar Mohanty, Jogeswar Panigrahi, et al.Hemoglobin|July 3, 2014
Known and new δ-globin gene mutations and other factors influencing Hb A2 measurement in the Omani populationSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.Hemoglobin|January 1, 1990
Enzyme immunoassay for the identification of hemoglobin variantsH Moscoso, C R Kiefer, M Shyamala, et al.Hemoglobin|June 28, 2012
The IVS-II-837 (T>G) appears to be a relatively common 'rare' β-globin gene mutation in β-thalassemia patients in Karnataka State, South IndiaMurali D Bashyam, Ajay K Chaudhary, Vijay BhatHemoglobin|June 28, 2012
The +1,506 (A>C) mutation in the 3' untranslated region affects β-globin expressionMinako Hino, Hitomi Ito, Yasuhiro Yamashiro, et al.Hemoglobin|January 1, 1979
The separation of human globin chains by ion-exchange chromatography on CM-Sepharose CL-6BS J Sparham, E R HuehnsHemoglobin|June 27, 2020
The Spectrum of α-Thalassemia Mutations in Kurdistan Province, West IranReza Alibakhshi, Keivan Moradi, Mozaffar Aznab, et al.Hemoglobin|June 27, 2020
Genotype-Phenotype Correlation of β-Thalassemia in Malaysian Population: Toward Effective Genetic CounselingUday Y H Abdullah, Hishamshah M Ibrahim, Noraesah Binti Mahmud, et al.Pageof 238