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Journal Abstract Search

303 related items for PubMed ID: 6208362

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  • 2. 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; 66(2-3):151-6. PubMed ID: 6201431
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  • 3. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.
    Losekoot M, Fodde R, Gerritsen EJ, van de Kuit I, Schreuder A, Giordano PC, Vossen JM, Bernini LF.
    Blood; 1991 Feb 15; 77(4):861-7. PubMed ID: 1704267
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  • 4. Characterisation of deletions which affect the expression of fetal globin genes in man.
    Fritsch EF, Lawn RM, Maniatis T.
    Nature; 1979 Jun 14; 279(5714):598-603. PubMed ID: 450109
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  • 6. Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFH.
    Soummer AM, Testa U, Dujardin P, Guerrasio A, Henri A, Gazaix M, Riou J, Rochant H, Beuzard Y, Rosa J.
    Hum Genet; 1981 Jun 14; 57(4):371-5. PubMed ID: 6169619
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  • 7. Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.
    Sofroniadou K, Wood WG, Nute PE, Stamatoyannopoulos G.
    Br J Haematol; 1975 Jan 14; 29(1):137-48. PubMed ID: 1201197
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  • 8. Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia trait.
    Garner C, Dew TK, Sherwood R, Rees D, Thein SL.
    Br J Haematol; 2003 Oct 14; 123(2):353-8. PubMed ID: 14531920
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  • 11. Heterocellular hereditary persistence of fetal haemoglobin (heterocellular HPFH) and its interaction with beta thalassaemia.
    Wood WG, Weatherall DJ, Clegg JB, Hamblin TJ, Edwards JH, Barlow AM.
    Br J Haematol; 1977 Aug 14; 36(4):461-73. PubMed ID: 889715
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  • 13. Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the beta globin gene complex.
    Donald JA, Lammi A, Trent RJ.
    Hum Genet; 1988 Sep 14; 80(1):69-74. PubMed ID: 2458313
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  • 16. Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II.
    Gurgey A, Kayin S, Kansu E, Altay C.
    J Med Genet; 1985 Jun 14; 22(3):213-21. PubMed ID: 2409284
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  • 19. Association of thalassaemia intermedia with a beta-globin gene haplotype.
    Thein SL, Wainscoat JS, Sampietro M, Old JM, Cappellini D, Fiorelli G, Modell B, Weatherall DJ.
    Br J Haematol; 1987 Mar 14; 65(3):367-73. PubMed ID: 2436649
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  • 20. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
    Ottolenghi S, Giglioni B, Taramelli R, Comi P, Mazza U, Saglio G, Camaschella C, Izzo P, Cao A, Galanello R, Gimferrer E, Baiget M, Gianni AM.
    Proc Natl Acad Sci U S A; 1982 Apr 14; 79(7):2347-51. PubMed ID: 6179097
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