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Hemoglobin|November 28, 2012
Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six casesCeleste Bento, Ana Catarina Oliveira, Joana Neves, et al.Hemoglobin|November 16, 2013
Newborn screening for Hb H disease by determination of Hb Bart's using the Sebia capillary electrophoresis system in southern ChinaCan Liao, Jian-Ying Zhou, Xing-Mei Xie, et al.Hemoglobin|November 27, 2013
Molecular and cellular analysis of a novel HBA2 mutation (HBA2: c.94A > G) shows activation of a cryptic splice site and generation of a premature termination codonTalal Qadah, Jill Finlayson, Philippe Joly, et al.Hemoglobin|November 9, 2013
Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in CisStacy Colaco, Amee Trivedi, Roshan B Colah, et al.Hemoglobin|November 12, 2013
Half of the Emirati population has abnormal red cell parameters: challenges for standards and screening guidelinesBayan Al-Dabbagh, Saad Shawqi, Javed Yasin, et al.Hemoglobin|January 1, 1986
Hb F-Urumqi G gamma I22(B4)Asp----Gly: a new fetal hemoglobin variant found in a Uygur babyH Y Hu, M S MaHemoglobin|November 6, 2014
Molecular spectrum of α-globin gene defects in the Omani populationSuha M Hassan, Cornelis L Harteveld, Egbert Bakker, et al.Hemoglobin|October 28, 2014
Molecular characterization and phenotypical study of β-thalassemia in Tucumán, ArgentinaSandra S Lazarte, María E Mónaco, Ana C Haro, et al.Hemoglobin|October 14, 2014
A systematic review and meta-analysis of deferiprone monotherapy and in combination with deferoxamine for reduction of iron overload in chronically transfused patients with β-thalassemiaKevin H M Kuo, Marko MrkobradaHemoglobin|May 25, 2026
Unstable Hemoglobin Variants: Molecular Mechanisms, Clinical Phenotypes, and a Practical Diagnostic and Management ApproachAikaterini Poulaki, Sophia DelicouPageof 239