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Journal Abstract Search

257 related items for PubMed ID: 2346726

  • 1. 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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  • 2. Promoter mutations producing mild beta-thalassaemia in the Italian population.
    Meloni A, Rosatelli MC, Faà V, Sardu R, Saba L, Murru S, Sciarratta GV, Baldi M, Tannoia N, Vitucci A.
    Br J Haematol; 1992 Feb; 80(2):222-6. PubMed ID: 1550780
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  • 7. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia.
    Camaschella C, Bertero MT, Serra A, Dall'Acqua M, Gasparini P, Trento M, Vettore L, Perona G, Saglio G, Mazza U.
    Br J Haematol; 1987 May; 66(1):103-7. PubMed ID: 3593644
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  • 8. Molecular characterization of beta-globin gene mutations in patients with beta-thalassaemia intermedia in south China.
    Antonarakis SE, Kang J, Lam VM, Tam JW, Li AM.
    Br J Haematol; 1988 Nov; 70(3):357-61. PubMed ID: 3207629
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  • 11. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
    Chen XW, Mo QH, Li Q, Zeng R, Xu XM.
    Ann Hematol; 2007 Sep; 86(9):653-7. PubMed ID: 17516066
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  • 13. 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 Sep; 316B():113-21. PubMed ID: 2482492
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  • 14. Severe thalassaemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for beta zero-thalassaemia.
    Oron V, Filon D, Oppenheim A, Rund D.
    Br J Haematol; 1994 Feb; 86(2):377-9. PubMed ID: 8199028
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  • 16. Thalassaemia intermedia: interaction of the triple alpha-globin gene arrangement and heterozygous beta-thalassaemia.
    Kulozik AE, Thein SL, Wainscoat JS, Gale R, Kay LA, Wood JK, Weatherall DJ, Huehns ER.
    Br J Haematol; 1987 May; 66(1):109-12. PubMed ID: 3593645
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  • 17. Heterozygous beta-thalassemia with thalassemia intermedia phenotype.
    Gasperini D, Perseu L, Melis MA, Maccioni L, Sollaino MC, Paglietti E, Cao A, Galanello R.
    Am J Hematol; 1998 Jan; 57(1):43-7. PubMed ID: 9423815
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  • 19. Thalassemia intermedia: moderate reduction of beta globin gene transcriptional activity by a novel mutation of the proximal CACCC promoter element.
    Kulozik AE, Bellan-Koch A, Bail S, Kohne E, Kleihauer E.
    Blood; 1991 May 01; 77(9):2054-8. PubMed ID: 2018842
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