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Journal Abstract Search

142 related items for PubMed ID: 2409869

  • 41.
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  • 42. Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.
    Bouva MJ, Harteveld CL, Bakker-Verweij G, van Delft P, Giordano PC.
    Hemoglobin; 2006; 30(3):371-7. PubMed ID: 16840228
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  • 43. Genetic heterogeneity of thalassemias in Mexican mestizo patients with hemolytic anemia.
    Ibarra B, Vaca G, de la Mora E, Romero F, Aguilar-Luna C, Mejía A, Esparza MA, Pérez G, Ornelas ML, Cantú JM.
    Hum Hered; 1988; 38(2):95-100. PubMed ID: 2454217
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  • 45. Globin gene mapping in normal Hb A2 types of beta-thalassaemia.
    Kanavakis E, Metaxotou-Mavromati A, Kattamis C, Aksoy M, Weatherall DJ, Wood WG.
    Br J Haematol; 1982 May; 51(1):59-64. PubMed ID: 7073990
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  • 52. A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and beta-thalassemia compound heterozygotes.
    Papadakis MN, Patrinos GP, Tsaftaridis P, Loutradi-Anagnostou A.
    J Mol Med (Berl); 2002 Apr; 80(4):243-7. PubMed ID: 11976733
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  • 53. Thalassemia revisited.
    Weatherall DJ, Clegg JB.
    Cell; 1982 May; 29(1):7-9. PubMed ID: 6179632
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  • 54. Gene deletion in hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia.
    Mears JG.
    Tex Rep Biol Med; 1982 May; 40():365-72. PubMed ID: 6172870
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  • 55. An erythroid-specific DNA binding factor mediates increased gamma-globin expression in hereditary persistence of fetal hemoglobin (HPFH).
    Martin DI, Orkin SH.
    Prog Clin Biol Res; 1989 May; 316A():217-28. PubMed ID: 2480608
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  • 56. Thalassemia types in Latium.
    Bianco I, Graziani B, Lerone M, Congedo P, Valente M, Ponzini D.
    Birth Defects Orig Artic Ser; 1982 May; 18(7):141-5. PubMed ID: 6186308
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  • 57. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL, Weatherall DJ.
    Prog Clin Biol Res; 1989 May; 316B():97-111. PubMed ID: 2482508
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