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Hemoglobin|January 20, 2026
Mild Thalassemic Effect of Heterozygous Hb Sogn in a Large Cohort from Routine Hemoglobinopathy InvestigationBente Fjeld, Markus Jørgensen, Paul Kjetel Soldal Lillemoen, et al.Hemoglobin|March 19, 1999
Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb Antananarivo [alpha1(NA1)Val-->Gly] and Hb Barbizon [beta144(HC1)Lys-->Met]J Kister, C Préhu, J Riou, et al.Hemoglobin|March 19, 1999
Genetic studies suggest a multicentric origin for Hb G-Coushatta [beta22(B4)Glu-->Ala]J Li, D Wilson, M Plonczynski, et al.Hemoglobin|May 9, 2013
Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: a new low oxygen affinity β chain variantRachel M Taliercio, Rendell W Ashton, Leonard Horwitz, et al.Hemoglobin|April 16, 2013
Evaluation and comparison of soluble transferrin receptor in thalassemia carriers and iron deficient patientsShohreh Khatami, Soghra Rouhi Dehnabeh, Ehsan Mostafavi, et al.Hemoglobin|January 1, 1990
Direct demonstration of the HB Suan-Dok mutation in the alpha 2-globin gene by restriction analysis with Sma IJ Hundrieser, T Sanguansermsri, M Laig, et al.Hemoglobin|December 11, 2012
Safety and efficacy of 4 years of deferasirox treatment for sickle cell disease patientsEfthymia Vlachaki, Maria Mainou, Eleni Bekiari, et al.Hemoglobin|January 29, 2013
Hb Treviso [α91(FG3)Leu→Phe (α2)]: a new slightly unstable hemoglobin variant with moderately decreased oxygen affinityGiuseppina Barberio, Daniela Leone, Giovanni Ivaldi, et al.Hemoglobin|December 14, 2012
Homozygosity for the severe β(+)-thalassemia mutation [IVS-I-5 (G>C)] causes the phenotype of thalassemia trait: an extremely rare presentationVinaykumar Bohara, Lalit Raut, Girish Badarkhe, et al.Hemoglobin|December 14, 2012
Detection of coinherited Hb H-Constant Spring/Paksé disease and Hb E by capillary electrophoresis and high performance liquid chromatographySakorn Pornprasert, Jarurin WaneesornPageof 238