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Journal Abstract Search

202 related items for PubMed ID: 1487426

  • 1. Hemoglobinopathies in Yugoslavia: an update.
    Efremov GD.
    Hemoglobin; 1992; 16(6):531-44. PubMed ID: 1487426
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  • 2. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
    [Abstract] [Full Text] [Related]

  • 3. Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian.
    Efremov GD.
    Haematologica; 1990; 75 Suppl 5():31-41. PubMed ID: 2086380
    [Abstract] [Full Text] [Related]

  • 4. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
    Indrák K, Divoký V, Brabec V, Indráková J, Svobodová M, Huisman TH.
    Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
    [Abstract] [Full Text] [Related]

  • 5. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
    Yuzbasioglu Ariyurek S, Yildiz SM, Yalin AE, Guzelgul F, Aksoy K.
    Hemoglobin; 2016 Jun; 40(3):168-72. PubMed ID: 26984585
    [Abstract] [Full Text] [Related]

  • 6. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016 Jun; 40(2):75-84. PubMed ID: 26635043
    [Abstract] [Full Text] [Related]

  • 7. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H.
    Hemoglobin; 2007 Jun; 31(4):463-9. PubMed ID: 17994380
    [Abstract] [Full Text] [Related]

  • 8. Molecular basis of beta-thalassemia and other hemoglobinopathies in Bulgaria: an update.
    Petkov GH, Efremov GD.
    Hemoglobin; 2007 Jun; 31(2):225-32. PubMed ID: 17486505
    [Abstract] [Full Text] [Related]

  • 9. Molecular Epidemiology of Hemoglobinopathies in Cambodia.
    Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, George J, Devenish R, Fucharoen S, Svasti S.
    Hemoglobin; 2016 Jun; 40(3):163-7. PubMed ID: 27117566
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  • 14. Globin mRNA in beta-thalassemia heterozygotes with different beta-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin.
    Smetanina NS, Adekile AD, Huisman TH.
    Acta Haematol; 1996 Jun; 96(3):162-9. PubMed ID: 8876614
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  • 18. Molecular characterization and phenotypical study of β-thalassemia in Tucumán, Argentina.
    Lazarte SS, Mónaco ME, Haro AC, Jiménez CL, Ledesma Achem ME, Issé BA.
    Hemoglobin; 2014 Jun; 38(6):394-401. PubMed ID: 25347257
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  • 19. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S, Fucharoen G.
    Hemoglobin; 2012 Jun; 36(1):18-24. PubMed ID: 22145566
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  • 20. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification.
    Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL.
    Blood; 1994 Mar 15; 83(6):1673-82. PubMed ID: 7510147
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