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Journal Abstract Search

758 related items for PubMed ID: 21204041

  • 1. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.
    Basak AN, Tuzmen S.
    Methods Mol Biol; 2011; 700():291-307. PubMed ID: 21204041
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  • 2. Prenatal diagnosis of hemoglobinopathies in Hacettepe University, Turkey.
    Beksac MS, Gumruk F, Gurgey A, Cakar N, Mumusoglu S, Ozyuncu O, Altay C.
    Pediatr Hematol Oncol; 2011 Feb; 28(1):51-5. PubMed ID: 20863160
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  • 3. A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders.
    Perrine SP, Ginder GD, Faller DV, Dover GH, Ikuta T, Witkowska HE, Cai SP, Vichinsky EP, Olivieri NF.
    N Engl J Med; 1993 Jan 14; 328(2):81-6. PubMed ID: 7677966
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  • 4. Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disorders.
    Pereira Mdel M, Dalmau AC, Corrons JL.
    Hemoglobin; 2009 Jan 14; 33(3):226-34. PubMed ID: 19657837
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  • 5. Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey.
    Mendilcioglu I, Yakut S, Keser I, Simsek M, Yesilipek A, Bagci G, Luleci G.
    Hemoglobin; 2011 Jan 14; 35(1):47-55. PubMed ID: 21250881
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  • 6. Premarital screening test results for β-thalassemia and sickle cell anemia trait in east Mediterranean region of Turkey.
    Guler E, Garipardic M, Dalkiran T, Davutoglu M.
    Pediatr Hematol Oncol; 2010 Nov 14; 27(8):608-13. PubMed ID: 20795773
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.
    Cürük MA, Zeren F, Genç A, Ozavci-Aygün S, Kilinç Y, Aksoy K.
    Hemoglobin; 2008 Nov 14; 32(6):525-30. PubMed ID: 19065329
    [Abstract] [Full Text] [Related]

  • 8. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia.
    Kan YW.
    Schweiz Med Wochenschr Suppl; 1991 Nov 14; 43():51-4. PubMed ID: 1726857
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  • 10. Novel and known microsatellite markers within the β-globin cluster to support robust preimplantation genetic diagnosis of β-thalassemia and sickle cell syndromes.
    Zachaki S, Vrettou C, Destouni A, Kokkali G, Traeger-Synodinos J, Kanavakis E.
    Hemoglobin; 2011 Nov 14; 35(1):56-66. PubMed ID: 21250882
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  • 13. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR, Martins ML, Brito AM, Rodrigues CV, Silva CM, Viana MB.
    Acta Haematol; 2010 Nov 14; 124(3):162-70. PubMed ID: 20938172
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  • 17. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH.
    Eur J Haematol; 2007 Jan 14; 78(1):82-5. PubMed ID: 17038017
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  • 18. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
    Bollekens JA, Forget BG.
    Hematol Oncol Clin North Am; 1991 Jun 14; 5(3):399-422. PubMed ID: 1713909
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  • 19. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 14; 64(4):1024-32. PubMed ID: 479366
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