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Hemoglobin|September 22, 2010
Severe β-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) β(+)-thalassemia mutation and the δ(0)β(+)-Senegalese deletionCéline Griffon, Philippe Joly, Agathe Sénéchal, et al.Hemoglobin|January 1, 1990
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantitiesM Harkness, D R Harkness, F Kutlar, et al.Hemoglobin|February 12, 2009
Newer aspects of the pathophysiology of sickle cell disease vaso-occlusionNicola Conran, Carla F Franco-Penteado, Fernando F CostaHemoglobin|February 12, 2009
Prenatal diagnosis of beta-thalassemia/Hb E by hemoglobin typing compared to DNA analysisSupatra Sirichotiyakul, Rattika Saetung, Torpong SanguansermsriHemoglobin|February 12, 2009
Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problemNassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, et al.Hemoglobin|February 12, 2009
Molecular characterization of alpha-thalassemia in the Dohuk region of IraqNasir A S Al-Allawi, Ameer I A Badi, Hasham Imanian, et al.Hemoglobin|February 12, 2009
Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variantJohn S Waye, Lynda Walker, Lisa M Nakamura, et al.Hemoglobin|February 12, 2009
Homozygosity for a rare beta 0-thalassemia mutation [frameshift codons 25/26 (+T)] causes beta-thalassemia intermedia in an Iranian familyMehdi Haghi, Abbas A Hosseinpour Feizi, Cornelis L Harteveld, et al.Hemoglobin|March 23, 2011
Identical mutations in the paralogous human γ-globin genes leading to hemoglobin variants and nondeletional hereditary persistence of fetal hemoglobinAdamantia Papachatzopoulou, George P PatrinosHemoglobin|March 23, 2011
Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia traitChi-Chiu So, Amy Y Y Chan, Hong-Yuan Luo, et al.Pageof 240