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Journal Abstract Search

169 related items for PubMed ID: 2458154

  • 21. Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.
    Tuan D, Feingold E, Newman M, Weissman SM, Forget BG.
    Proc Natl Acad Sci U S A; 1983 Nov; 80(22):6937-41. PubMed ID: 6196781
    [Abstract] [Full Text] [Related]

  • 22. A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia.
    Kulozik AE, Bellan-Koch A, Kohne E, Kleihauer E.
    Blood; 1992 May 01; 79(9):2455-9. PubMed ID: 1571556
    [Abstract] [Full Text] [Related]

  • 23. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
    Feingold EA, Forget BG.
    Blood; 1989 Nov 01; 74(6):2178-86. PubMed ID: 2478223
    [Abstract] [Full Text] [Related]

  • 24. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification.
    Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL.
    Blood; 1994 Mar 15; 83(6):1673-82. PubMed ID: 7510147
    [Abstract] [Full Text] [Related]

  • 25. A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
    Henthorn PS, Mager DL, Huisman TH, Smithies O.
    Proc Natl Acad Sci U S A; 1986 Jul 15; 83(14):5194-8. PubMed ID: 2425363
    [Abstract] [Full Text] [Related]

  • 26. Homozygosity for a new type of G gamma (A gamma delta beta)zero-thalassemia in a Malaysian male.
    George E, Faridah K, Trent RJ, Padanilam BJ, Huang HJ, Huisman TH.
    Hemoglobin; 1986 Jul 15; 10(4):353-63. PubMed ID: 2427478
    [Abstract] [Full Text] [Related]

  • 27. A novel deletion in delta beta-thalassemia found in Japan.
    Matsunaga E, Kimura A, Yamada H, Fukumaki Y, Takagi Y.
    Biochem Biophys Res Commun; 1985 Jan 16; 126(1):185-91. PubMed ID: 2982369
    [Abstract] [Full Text] [Related]

  • 28. Dutch beta 0-thalassaemia: a 10 kilobase DNA deletion associated with significant gamma-chain production.
    Gilman JG, Huisman TH, Abels J.
    Br J Haematol; 1984 Feb 16; 56(2):339-48. PubMed ID: 6318797
    [Abstract] [Full Text] [Related]

  • 29. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R, Podda A, Melis MA, Monne M, Cao A.
    Prog Clin Biol Res; 1989 Feb 16; 316B():113-21. PubMed ID: 2482492
    [Abstract] [Full Text] [Related]

  • 30. A patient of German descent with (delta beta)0-thalassemia carrying the Sicilian type deletion of the delta and beta globin genes.
    Hopmeier P, Shenhav A, Glaser G, Rachmilewitz EA, Oppenheim A.
    Hemoglobin; 1988 Feb 16; 12(1):39-51. PubMed ID: 3384697
    [Abstract] [Full Text] [Related]

  • 31. Recombination at the human alpha-globin gene cluster: sequence features and topological constraints.
    Nicholls RD, Fischel-Ghodsian N, Higgs DR.
    Cell; 1987 May 08; 49(3):369-78. PubMed ID: 3032452
    [Abstract] [Full Text] [Related]

  • 32. The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence.
    Mishima N, Landman H, Huisman TH, Gilman JG.
    Br J Haematol; 1989 Nov 08; 73(3):375-9. PubMed ID: 2605124
    [Abstract] [Full Text] [Related]

  • 33. Delta-beta-thalassemia is due to a gene deletion.
    Ottolenghi S, Comi P, Giglioni B, Tolstoshev P, Lanyon WG, Mitchell GJ, Williamson R, Russo G, Musumeci S, Schillro G, Tsistrakis GA, Charache S, Wood WG, Clegg JB, Weatherall DJ.
    Cell; 1976 Sep 08; 9(1):71-80. PubMed ID: 975241
    [Abstract] [Full Text] [Related]

  • 34. Gene analysis in delta beta and delta (0) thalassemia.
    Baird M, Driscoll MC, Ben-Bassat I, Ohta Y, Nakamura F, Bloom A, Bank A.
    J Biol Chem; 1984 Jan 10; 259(1):512-5. PubMed ID: 6323412
    [Abstract] [Full Text] [Related]

  • 35. Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
    Vives-Corrons JL, Pujades MA, Miguel-García A, Miguel-Sosa A, Cambiazzo S.
    Blood; 1992 Sep 15; 80(6):1582-5. PubMed ID: 1520881
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  • 39. A distant gene deletion affects beta-globin gene function in an atypical gamma delta beta-thalassemia.
    Curtin P, Pirastu M, Kan YW, Gobert-Jones JA, Stephens AD, Lehmann H.
    J Clin Invest; 1985 Oct 15; 76(4):1554-8. PubMed ID: 2997283
    [Abstract] [Full Text] [Related]

  • 40. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.
    Giampaolo A, Mavilio F, Sposi NM, Carè A, Massa A, Cianetti L, Petrini M, Russo R, Cappellini MD, Marinucci M.
    Hum Genet; 1984 Oct 15; 66(2-3):151-6. PubMed ID: 6201431
    [Abstract] [Full Text] [Related]

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