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Journal Abstract Search

181 related items for PubMed ID: 1482661

  • 21. A Family with γ-Thalassemia and High Hb A2 Levels.
    Parmeggiani G, Gualandi F, Selvatici R, Rimessi P, Bigoni S, Taddei Masieri M, Dolcini B, Venturoli A, Cappabianca MP, Ferlini A, Ravani A.
    Hemoglobin; 2016 Jun; 40(3):187-90. PubMed ID: 27117568
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  • 22. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
    So CC, Chan AY, Tsang ST, Lee AC, Au WY, Ma ES, Chan LC.
    Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
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  • 24. A beta-thalassaemia phenotype not linked to the beta-globin cluster in an Italian family.
    Murru S, Loudianos G, Porcu S, Sciarratta GV, Agosti S, Parodi MI, Cao A, Pirastu M.
    Br J Haematol; 1992 Jun; 81(2):283-7. PubMed ID: 1643026
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  • 25. 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; 127(5):604-6. PubMed ID: 15566365
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  • 26. Physical mapping of the globin gene deletion in (delta beta (0)) -thalassaemia.
    Bernards R, Kooter JM, Flavell RA.
    Gene; 1979 Jul; 6(3):265-80. PubMed ID: 478302
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  • 33. A large beta-thalassemia deletion in a family of Indonesian-Malay descent.
    Dimovski AJ, Baysal E, Efremov DG, Prior JF, Raven JL, Efremov GD, Huisman TH.
    Hemoglobin; 1996 Nov; 20(4):377-92. PubMed ID: 8936464
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  • 34. The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian population.
    Ristaldi MS, Murru S, Loudianos G, Casula L, Porcu S, Pigheddu D, Fanni B, Sciarratta GV, Agosti S, Parodi MI.
    Br J Haematol; 1990 Apr; 74(4):480-6. PubMed ID: 2346726
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  • 35. Molecular characterization of an atypical beta-thalassemia caused by a large deletion in the 5' beta-globin gene region.
    Popovich BW, Rosenblatt DS, Kendall AG, Nishioka Y.
    Am J Hum Genet; 1986 Dec; 39(6):797-810. PubMed ID: 3799598
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  • 36. High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemia.
    Patterson M, Walker L, Eng B, Waye JS.
    Hemoglobin; 2005 Dec; 29(4):293-5. PubMed ID: 16370492
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  • 37. Characterization of an Indian (delta beta)0 thalassaemia.
    Wainscoat JS, Old JM, Wood WG, Trent RJ, Weatherall DJ.
    Br J Haematol; 1984 Oct; 58(2):353-60. PubMed ID: 6477837
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  • 39. 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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