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Journal Abstract Search

256 related items for PubMed ID: 23281611

  • 1. Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemia.
    Lacerra G, Prezioso R, Musollino G, Piluso G, Mastrullo L, De Angioletti M.
    Eur J Haematol; 2013 Mar; 90(3):214-9. PubMed ID: 23281611
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  • 4. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
    Singha K, Fucharoen G, Hama A, Fucharoen S.
    Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
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  • 7. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
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  • 8. Molecular characterization of a beta-globin gene deletion of 1357 bp in a Taiwanese beta-thalassemia carrier.
    Huang CH, Chang YY, Chen CH, Ko TM.
    Hemoglobin; 2008 Jan; 32(5):498-504. PubMed ID: 18932076
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  • 10. Mild beta-thalassemia intermedia caused by compound heterozygosity for (G)gamma((A)gammadeltabeta)(o)/beta-thalassemia and molecular characterization of the defect in four Chinese families.
    Tan Jin Ai MA, Yap SF, Tan KL, Wong YC, Wee YC, Kok JL.
    Acta Haematol; 2003 Jan; 109(4):169-75. PubMed ID: 12853688
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  • 11. Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.
    Lou JW, Li Q, Wei XF, Huang JW, Xu XM.
    Hemoglobin; 2010 Jan; 34(4):343-53. PubMed ID: 20642332
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  • 14. Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.
    Waye JS, Eng B, Got T, Hanna M, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2015 Jan; 39(5):368-70. PubMed ID: 26154945
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  • 15. Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
    Gallienne AE, Iberson NM, Dréau HM, Jackson H, Bignell PA, Old JM, Schuh A, Henderson SJ.
    Hemoglobin; 2010 Jan; 34(1):110-4. PubMed ID: 20113295
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  • 17. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
    Jiang F, Zuo L, Li D, Li J, Tang X, Chen G, Zhou J, Lu H, Liao C.
    BMC Med Genet; 2020 Feb 28; 21(1):43. PubMed ID: 32111191
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  • 18. Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.
    Joly P, Lacan P, Garcia C, Couprie N, Francina A.
    Blood Cells Mol Dis; 2009 Feb 28; 43(1):53-7. PubMed ID: 19269866
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