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Journal Abstract Search

221 related items for PubMed ID: 19205970

  • 1. Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem.
    Boudrahem-Addour N, Zidani N, Carion N, Labie D, Belhani M, Beldjord C.
    Hemoglobin; 2009; 33(1):24-36. PubMed ID: 19205970
    [Abstract] [Full Text] [Related]

  • 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. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A.
    Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
    [Abstract] [Full Text] [Related]

  • 4. The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
    Kiani AA, Mortazavi Y, Zeinali S, Shirkhani Y.
    Hemoglobin; 2007; 31(3):343-9. PubMed ID: 17654071
    [Abstract] [Full Text] [Related]

  • 5. The molecular heterogeneity of beta-thalassemia in Greece.
    Boussiou M, Karababa P, Sinopoulou K, Tsaftaridis P, Plata E, Loutradi-Anagnostou A.
    Blood Cells Mol Dis; 2008; 40(3):317-9. PubMed ID: 18096416
    [Abstract] [Full Text] [Related]

  • 6. Distribution of beta-thalassemia mutations in the northern provinces of Iran.
    Derakhshandeh-Peykar P, Akhavan-Niaki H, Tamaddoni A, Ghawidel-Parsa S, Naieni KH, Rahmani M, Babrzadeh F, Dilmaghani-Zadeh M, Farhud DD.
    Hemoglobin; 2007; 31(3):351-6. PubMed ID: 17654072
    [Abstract] [Full Text] [Related]

  • 7. Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
    Salehi R, Fisher CA, Bignell PA, Eslami G, Old JM.
    Hemoglobin; 2010; 34(1):115-20. PubMed ID: 20113296
    [Abstract] [Full Text] [Related]

  • 8. Molecular characterization of beta-thalassemia in the Dohuk region of Iraq.
    Al-Allawi NA, Jubrael JM, Hughson M.
    Hemoglobin; 2006; 30(4):479-86. PubMed ID: 16987803
    [Abstract] [Full Text] [Related]

  • 9. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 10. Diversity of the 5' beta-globin haplotype of four beta-thalassemia mutations in the Mexican population.
    Morales KR, Magaña MT, Ibarra B, Perea FJ.
    Hemoglobin; 2009; 33(1):66-71. PubMed ID: 19205976
    [Abstract] [Full Text] [Related]

  • 11. Molecular updating of β-thalassemia mutations in the Upper Egyptian population.
    Jiffri EH, Bogari N, Zidan KH, Teama S, Elhawary NA.
    Hemoglobin; 2010; 34(6):538-47. PubMed ID: 21077761
    [Abstract] [Full Text] [Related]

  • 12. Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.
    Makhoul NJ, Wells RS, Kaspar H, Shbaklo H, Taher A, Chakar N, Zalloua PA.
    Ann Hum Genet; 2005 Jan; 69(Pt 1):55-66. PubMed ID: 15638828
    [Abstract] [Full Text] [Related]

  • 13. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007 Jan; 31(2):233-41. PubMed ID: 17486506
    [Abstract] [Full Text] [Related]

  • 14. Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.
    Agouti I, Badens C, Abouyoub A, Khattab M, Sayah F, Barakat A, Bennani M.
    Hemoglobin; 2007 Jan; 31(2):141-9. PubMed ID: 17486495
    [Abstract] [Full Text] [Related]

  • 15. Origin of the frameshift codons 41/42 (-TCTT) mutation in the first cases described in the Spanish population.
    Ropero P, de la Iglesia S, Calvo-Villas JM, González FA, Paúl R, Villegas A.
    Hemoglobin; 2008 Jan; 32(5):513-9. PubMed ID: 18932079
    [Abstract] [Full Text] [Related]

  • 16. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
    Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R.
    Hemoglobin; 2012 Jan; 36(3):209-18. PubMed ID: 22563936
    [Abstract] [Full Text] [Related]

  • 17. Molecular basis of beta-thalassemia in the population of Tunisia.
    Fattoum S, Messaoud T, Bibi A.
    Hemoglobin; 2004 Aug; 28(3):177-87. PubMed ID: 15481884
    [Abstract] [Full Text] [Related]

  • 18. Molecular basis of β-thalassemia in the western province of Saudi Arabia: identification of rare β-thalassemia mutations.
    Abuzenadah AM, Hussein IM, Damanhouri GA, A-Sayes FM, Gari MA, Chaudhary AG, Zaher GF, Al-Attas A, Al-Qahtani MH.
    Hemoglobin; 2011 Aug; 35(4):346-57. PubMed ID: 21797702
    [Abstract] [Full Text] [Related]

  • 19. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
    Kukreti R, Dash D, E VK, Chakravarty S, Das SK, De M, Talukder G.
    Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
    [Abstract] [Full Text] [Related]

  • 20. beta-Thalassemia mutations in the Iranian Kurdish population of Kurdistan and West Azerbaijan provinces.
    Haghi M, Khorshidi S, Hosseinpour Feizi MA, Pouladi N, Hosseinpour Feizi AA.
    Hemoglobin; 2009 Aug; 33(2):109-14. PubMed ID: 19373586
    [Abstract] [Full Text] [Related]

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