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617 related items for PubMed ID: 22686351

  • 1. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. The spectrum of β-thalassemia mutations in Baghdad, Central Iraq.
    Al-Allawi NA, Al-Mousawi BM, Badi AI, Jalal SD.
    Hemoglobin; 2013; 37(5):444-53. PubMed ID: 23826747
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Beta-globin gene cluster haplotypes in sickle cell patients from southwest Iran.
    Rahimi Z, Karimi M, Haghshenass M, Merat A.
    Am J Hematol; 2003 Nov; 74(3):156-60. PubMed ID: 14587041
    [Abstract] [Full Text] [Related]

  • 6. Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará.
    De Lemos Cardoso G, Guerreiro JF.
    Am J Hum Biol; 2010 Nov; 22(5):573-7. PubMed ID: 20737602
    [Abstract] [Full Text] [Related]

  • 7. Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.
    Adekile AD, Gu LH, Baysal E, Haider MZ, al-Fuzae L, Aboobacker KC, al-Rashied A, Huisman TH.
    Acta Haematol; 1994 Nov; 92(4):176-81. PubMed ID: 7701914
    [Abstract] [Full Text] [Related]

  • 8. Haplotype analysis of beta thalassemia patients in Western Iran.
    Rahimi Z, Muniz A, Akramipour R, Tofieghzadeh F, Mozafari H, Vaisi-Raygani A, Parsian A.
    Blood Cells Mol Dis; 2009 Nov; 42(2):140-3. PubMed ID: 19141369
    [Abstract] [Full Text] [Related]

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

  • 10. 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 Nov; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 11. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
    Bibi A, Messaoud T, Fattoum S.
    Hemoglobin; 2006 Nov; 30(2):175-81. PubMed ID: 16798642
    [Abstract] [Full Text] [Related]

  • 12. 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 Nov; 34(5):461-8. PubMed ID: 20854120
    [Abstract] [Full Text] [Related]

  • 13. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
    Murad H, Moassas F, Jarjour R, Mukhalalaty Y, Al-Achkar W.
    Hemoglobin; 2014 Nov; 38(6):390-3. PubMed ID: 25405916
    [Abstract] [Full Text] [Related]

  • 14. 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 Nov; 33(1):66-71. PubMed ID: 19205976
    [Abstract] [Full Text] [Related]

  • 15. Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
    Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R.
    Blood Cells Mol Dis; 2009 Nov; 42(1):25-31. PubMed ID: 18954999
    [Abstract] [Full Text] [Related]

  • 16. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Daniel Y, Hill K, Inusa B, Thein SL, Howard J.
    Hemoglobin; 2011 Nov; 35(4):406-10. PubMed ID: 21797706
    [Abstract] [Full Text] [Related]

  • 17. Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan.
    Shamoon RP, Al-Allawi NA, Cappellini MD, Di Pierro E, Brancaleoni V, Granata F.
    Hemoglobin; 2015 Nov; 39(3):178-83. PubMed ID: 25902180
    [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 Nov; 35(4):346-57. PubMed ID: 21797702
    [Abstract] [Full Text] [Related]

  • 19. [Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese].
    Liu L, Jiang WY, Xu SY, Chen J, Chen LM, Tian QH, Wang JC.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Jul; 34(7):595-9. PubMed ID: 23906453
    [Abstract] [Full Text] [Related]

  • 20. beta(S)-Globin gene cluster haplotypes in the West Bank of Palestine.
    Samarah F, Ayesh S, Athanasiou M, Christakis J, Vavatsi N.
    Hemoglobin; 2009 Jul; 33(2):143-9. PubMed ID: 19373591
    [Abstract] [Full Text] [Related]

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