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Journal Abstract Search

361 related items for PubMed ID: 22734501

  • 1. The IVS-II-837 (T>G) appears to be a relatively common 'rare' β-globin gene mutation in β-thalassemia patients in Karnataka State, South India.
    Bashyam MD, Chaudhary AK, Bhat V.
    Hemoglobin; 2012; 36(5):497-503. PubMed ID: 22734501
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 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. [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]

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

  • 6. Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutations.
    Jarjour RA, Murad H, Moasses F, Al-Achkar W.
    Hemoglobin; 2014 Jul; 38(4):272-6. PubMed ID: 24828949
    [Abstract] [Full Text] [Related]

  • 7. Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece.
    Papachatzopoulou A, Kourakli A, Stavrou EF, Fragou E, Vantarakis A, Patrinos GP, Athanassiadou A.
    Hemoglobin; 2010 Jul; 34(4):333-42. PubMed ID: 20642331
    [Abstract] [Full Text] [Related]

  • 8. 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 Jul; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 9. Hb E/β-thalassemia: the second most common cause of transfusion-dependent thalassemia in the Gwalior-Chambal region of Central India.
    Kumar R, Sharma DC, Kishor P.
    Hemoglobin; 2012 Jul; 36(5):485-90. PubMed ID: 22738610
    [Abstract] [Full Text] [Related]

  • 10. Two novel mutations in the 3' untranslated region of the beta-globin gene that are associated with the mild phenotype of beta thalassemia.
    Bilgen T, Clark OA, Ozturk Z, Akif Yesilipek M, Keser I.
    Int J Lab Hematol; 2013 Feb; 35(1):26-30. PubMed ID: 22862814
    [Abstract] [Full Text] [Related]

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

  • 12. The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.
    Sirdah MM, Sievertsen J, Al-Yazji MS, Tarazi IS, Al-Haddad RM, Horstmann RD, Timmann C.
    Blood Cells Mol Dis; 2013 Apr; 50(4):247-51. PubMed ID: 23321370
    [Abstract] [Full Text] [Related]

  • 13. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Surve R, Subramaniam PG, Bondge N, Pujari K, Ghosh K, Mohanty D.
    Blood Cells Mol Dis; 2004 Apr; 33(2):153-7. PubMed ID: 15315795
    [Abstract] [Full Text] [Related]

  • 14. 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 Apr; 34(5):469-76. PubMed ID: 20854121
    [Abstract] [Full Text] [Related]

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

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

  • 17. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
    Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH.
    Hemoglobin; 2014 Apr; 38(1):24-7. PubMed ID: 24200152
    [Abstract] [Full Text] [Related]

  • 18. β-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study.
    Kurtoğlu A, Karakuş V, Erkal Ö, Kurtoğlu E.
    Hemoglobin; 2016 Nov; 40(6):392-395. PubMed ID: 28276871
    [Abstract] [Full Text] [Related]

  • 19. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [Abstract] [Full Text] [Related]

  • 20. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

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