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Hemoglobin|January 17, 2002
Hb Antalya [codons 3-5 (Leu-Thr-Pro-->Ser-Asp-Ser)]: a new unstable variant leading to chronic microcytic anemia and high Hb A2I Keser, O G Kayisli, A Yesilipek, et al.Hemoglobin|January 17, 2002
Hb Dartmouth [alpha66(E15)Leu-->Pro (alpha2) (CTG-->CCG)]: a novel alpha2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian alpha-thalassemia-1K L McBride, K Snow, K S Kubik, et al.Hemoglobin|January 17, 2002
Interaction of the alpha2 polyadenylation signal mutation (AATAAA-->AATA--) and alpha0-thalassemia (--SEA), resulting in Hb H disease in a Thai patientV Laosombat, S Fucharoen, A WiriyasateinkulHemoglobin|January 17, 2002
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patientE Birben, R Oner, C Oner, et al.Hemoglobin|July 30, 2002
Molecular characterization of Hb D-Ibadan [beta87(F3)Thr-->Lys] in combination with Hb S [beta6(A3)Glu-->Val] and with beta+-Thalassemia: report of two casesRupa Redding-Lallinger, Gaye Tankut, Leslie Holley, et al.Hemoglobin|July 30, 2002
Beta-thalassemia in the Korean populationSung Sup Park, Young Joon Lee, Ji Yeon Kim, et al.Hemoglobin|October 31, 2002
Coexistence of a novel beta-globin gene deletion (codons 81-87) with the codon 30 (G-->C) mutation in an Indian patient with beta0-thalassemiaRamachandran V Shaji, Alok Srivastava, Rajagopal Krishnamoorthy, et al.Hemoglobin|October 31, 2002
Hb Groene Hart: a new Pro-->Ser amino acid substitution at position 119 of the alpha1-globin chain is associated with a mild alpha-thalassemia phenotypeCornelis L Harteveld, Peter van Delft, Rob Plug, et al.Hemoglobin|December 18, 2002
Importance of helices A and H in oxygen binding differences between bovine and human hemoglobinsVéronique Baudin-Creuza, Corinne Vasseur-Godbillon, Jean Kister, et al.Hemoglobin|June 5, 2003
Origin of Hb A2' (Hb B2) [delta16(A13)Gly --> Arg (GGC --> CGC)]Mohcine Bennani, Landry-Erik Mombo, André Chaventre, et al.Pageof 240