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Journal Abstract Search

96 related items for PubMed ID: 16114183

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  • 3. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H.
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
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  • 6. A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
    Tritipsombut J, Phylipsen M, Viprakasit V, Chalaow N, Sanchaisuriya K, Giordano PC, Fucharoen S, Harteveld CL.
    Hemoglobin; 2012; 36(6):571-80. PubMed ID: 23181748
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  • 7. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
    Feriotto G, Salvatori F, Finotti A, Breveglieri G, Venturi M, Zuccato C, Bianchi N, Borgatti M, Lampronti I, Mancini I, Massei F, Favre C, Gambari R.
    Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
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  • 8. The 3' breakpoint of the yunnanese (Agammadeltabeta)0-thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the Ggamma-globin gene.
    Zhang XQ, Zhang JW.
    Hum Genet; 1998 Jul; 103(1):90-5. PubMed ID: 9737783
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  • 9. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA, Lanaro C, Albuquerque DM, Ferreira R, Costa FF.
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
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  • 12. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007 Feb; 31(1):1-15. PubMed ID: 17365000
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  • 14. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S, Fucharoen S, Surapot S, Fucharoen G, Sanchaisuriya K.
    Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
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  • 17. 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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  • 18. Application of multiplex ligation-dependent probe amplification to screen for β-globin cluster deletions: detection of two novel deletions in a multi ethnic population.
    Cui J, Azimi M, Baysdorfer C, Vichinsky EP, Hoppe CC.
    Hemoglobin; 2013 Mar; 37(3):241-56. PubMed ID: 23577918
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  • 19. Novel 112 kb (epsilonGgammaAgamma) deltabeta-thalassaemia deletion in a Dutch family.
    Harteveld CL, Osborne CS, Peters M, van der Werf S, Plug R, Fraser P, Giordano PC.
    Br J Haematol; 2003 Sep; 122(5):855-8. PubMed ID: 12930401
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  • 20. A novel epsilon gamma delta beta thalassemia of 1.4 Mb deletion found in a Japanese patient.
    Furuya C, Yamashiro Y, Hattori Y, Hino M, Nishioka H, Shimizu Y, Okano K, Horibe K.
    Am J Hematol; 2008 Jan; 83(1):84-6. PubMed ID: 17712794
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