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PUBMED FOR HANDHELDS

Journal Abstract Search


371 related items for PubMed ID: 20113296

  • 1. 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]

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  • 3. 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]

  • 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. 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]

  • 6. Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of Iran.
    Miri-Moghaddam E, Zadeh-Vakili A, Nikravesh A, Sistani SS, Naroie-Nejad M.
    Hemoglobin; 2013; 37(2):138-47. PubMed ID: 23437895
    [Abstract] [Full Text] [Related]

  • 7. Molecular spectrum of beta-thalassemia mutations in Northwestern Iran.
    Hosseinpour Feizi MA, Hosseinpour Feizi AA, Pouladi N, Haghi M, Azarfam P.
    Hemoglobin; 2008; 32(3):255-61. PubMed ID: 18473241
    [Abstract] [Full Text] [Related]

  • 8. 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; 33(2):109-14. PubMed ID: 19373586
    [Abstract] [Full Text] [Related]

  • 9. Profile of β-thalassemia and its prenatal diagnosis in Khorasan-e-Jonobi Province, Iran.
    Miri-Moghaddam E, Zadeh-Vakili A.
    Hemoglobin; 2012; 36(5):456-63. PubMed ID: 22920564
    [Abstract] [Full Text] [Related]

  • 10. 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; 36(3):209-18. PubMed ID: 22563936
    [Abstract] [Full Text] [Related]

  • 11. β-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.
    Rahiminejad MS, Zeinali S, Afrasiabi A, Valeshabad AK.
    Hemoglobin; 2011; 35(4):331-7. PubMed ID: 21797700
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. β-Thalassemia mutations in the Kurdish population of northeastern Iraq.
    Jalal SD, Al-Allawi NA, Bayat N, Imanian H, Najmabadi H, Faraj A.
    Hemoglobin; 2010; 34(5):469-76. PubMed ID: 20854121
    [Abstract] [Full Text] [Related]

  • 14. Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
    Hussein G, Fawzy M, Serafi TE, Ismail EF, Metwally DE, Saber MA, Giansily M, Schved JF, Pissard S, Martinez PA.
    Hemoglobin; 2007; 31(1):49-62. PubMed ID: 17365005
    [Abstract] [Full Text] [Related]

  • 15. Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.
    Galehdari H, Salehi B, Azmoun S, Keikhaei B, Zandian KM, Pedram M.
    Hemoglobin; 2010; 34(5):461-8. PubMed ID: 20854120
    [Abstract] [Full Text] [Related]

  • 16. Detection of beta-thalassemia mutations using a multiplex amplification refractory mutation system assay.
    Mirasena S, Shimbhu D, Sanguansermsri M, Sanguansermsri T.
    Hemoglobin; 2008; 32(4):403-9. PubMed ID: 18654891
    [Abstract] [Full Text] [Related]

  • 17. 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; 35(4):346-57. PubMed ID: 21797702
    [Abstract] [Full Text] [Related]

  • 18. Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.
    Ozkinay F, Onay H, Karaca E, Arslan E, Erturk B, Ece Solmaz A, Tekin IM, Cogulu O, Aydinok Y, Vergin C.
    Hemoglobin; 2015; 39(4):230-4. PubMed ID: 26076395
    [Abstract] [Full Text] [Related]

  • 19. Molecular basis of β-thalassemia in the United Arab Emirates.
    Baysal E.
    Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
    [Abstract] [Full Text] [Related]

  • 20. 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]


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