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PUBMED FOR HANDHELDS

Journal Abstract Search


217 related items for PubMed ID: 1419783

  • 21.
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  • 23. Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.
    Sanguansermsri T, Pape M, Laig M, Hundrieser J, Flatz G.
    Hemoglobin; 1990; 14(2):157-68. PubMed ID: 2272839
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  • 24. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
    Coleman MB, Adams JG, Plonczynski MW, Harrell AH, Walker AM, Fairbanks V, Steinberg MH.
    Am J Med Sci; 1992 Aug; 304(2):73-8. PubMed ID: 1380206
    [Abstract] [Full Text] [Related]

  • 25. 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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  • 27. Molecular analysis of a thai beta-thalassaemia heterozygote with normal haemoglobin A2 level: implication for population screening.
    Fucharoen S, Fucharoen G, Sanchaisuriya K, Pengjam Y.
    Ann Clin Biochem; 2002 Jan; 39(Pt 1):44-9. PubMed ID: 11853188
    [Abstract] [Full Text] [Related]

  • 28. A beta-thalassemia variant associated with unusually high hemoglobin A2 in an Iranian family.
    Thein SL, Barnetson R, Abdalla S.
    Blood; 1992 May 15; 79(10):2801-3. PubMed ID: 1586730
    [No Abstract] [Full Text] [Related]

  • 29. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
    Galanello R, Perseu L, Perra C, Maccioni L, Barella S, Longinotti M, Cao A, Cazzola M.
    Br J Haematol; 2004 Dec 15; 127(5):604-6. PubMed ID: 15566365
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  • 30. Characterization of an Indian (delta beta)0 thalassaemia.
    Wainscoat JS, Old JM, Wood WG, Trent RJ, Weatherall DJ.
    Br J Haematol; 1984 Oct 15; 58(2):353-60. PubMed ID: 6477837
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  • 31. Beta + thalassemia--Portuguese type: clinical, haematological and molecular studies of a newly defined form of beta thalassaemia.
    Tamagnini GP, Lopes MC, Castanheira ME, Wainscoat JS, Wood WG.
    Br J Haematol; 1983 Jun 15; 54(2):189-200. PubMed ID: 6189507
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  • 32. Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.
    Altay C, Gurgey A.
    J Med Genet; 1985 Jun 15; 22(3):205-12. PubMed ID: 2409283
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  • 35. Characterization of a new alpha-thalassemia-1 deletion in a Spanish family.
    Gonzalez-Redondo JM, Gilsanz F, Ricard P.
    Hemoglobin; 1989 Jun 15; 13(2):103-16. PubMed ID: 2544542
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  • 36.
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  • 37. Globin gene mapping in normal Hb A2 types of beta-thalassaemia.
    Kanavakis E, Metaxotou-Mavromati A, Kattamis C, Aksoy M, Weatherall DJ, Wood WG.
    Br J Haematol; 1982 May 15; 51(1):59-64. PubMed ID: 7073990
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  • 38.
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  • 39. Physical mapping of the globin gene deletion in (delta beta (0)) -thalassaemia.
    Bernards R, Kooter JM, Flavell RA.
    Gene; 1979 Jul 15; 6(3):265-80. PubMed ID: 478302
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  • 40.
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