Showing results (1641-1650 of 2,379) with videos related to
Sort By:
Pageof 238
Hemoglobin|January 1, 1986
A study of the minor peaks in high performance liquid chromatograms of globin chains on reversed phase columnsW A Schroeder, J B Shelton, V Huynh, et al.Hemoglobin|July 18, 2020
Hematological Characteristics of β-Globin Gene Mutation -50 (G>A) (HBB: c.-100G>A) Carriers in Mainland ChinaYuan Zhao, Fan Jiang, Dong-Zhi LiHemoglobin|January 1, 1990
Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variantP C Giordano, R Fodde, R Amons, et al.Hemoglobin|January 1, 1990
Hb Mizuho [beta 68(E12)Leu----Pro]. Second occurrence identified in a Caucasian child with hemolytic anemia and dense erythrocyte inclusionsR J Labotka, L N Vida, G R HonigHemoglobin|January 1, 1990
Characterization of Hb Aalborg, a new unstable hemoglobin variant, by fast atom bombardment mass spectrometryD Williamson, J Nutkins, S Rosthoj, et al.Hemoglobin|January 1, 1990
Hb Johnstown [beta 109 (G11) Val----Leu]: a new electrophoretically silent variant that causes erythrocytosisR T Jones, H I Saiontz, C Head, et al.Hemoglobin|January 1, 1990
Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin geneT Sanguansermsri, M Pape, M Laig, et al.Hemoglobin|September 8, 1998
Partitioning of oxygen and carbon monoxide in the three human embryonic hemoglobinsO M Hofmann, T BrittainHemoglobin|January 1, 1979
Microchromatographic quantitation of fetal hemoglobin in patients with sickle cell diseaseE C Abraham, J Carver, J Döbler, et al.Hemoglobin|April 2, 2015
Usability and Feasibility of an mHealth Intervention for Monitoring and Managing Pain Symptoms in Sickle Cell Disease: The Sickle Cell Disease Mobile Application to Record Symptoms via Technology (SMART)Charles R Jonassaint, Nirmish Shah, Jude Jonassaint, et al.Pageof 238