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Journal Abstract Search

150 related items for PubMed ID: 6163196

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  • 2. The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newborn.
    Huisman TH, Efremov GD, Reese AL, Howard JS, Gravely ME, Harris HF, Wilson JB.
    Hemoglobin; 1979; 3(4):223-52. PubMed ID: 500369
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  • 3. Fetal hemoglobin synthesis in erythroid cultures in hereditary persistence of fetal hemoglobin and beta o-thalassemia.
    Weinberg RS, Antonarakis SE, Kazazian HH, Dover GJ, Orkin SH, Lenes AL, Schofield JM, Alter BP.
    Blood; 1984 Jun; 63(6):1278-84. PubMed ID: 6202341
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  • 4. 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; 22(3):213-21. PubMed ID: 2409284
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  • 5. beta Thalassemia associated with increased HB F production. Evidence for the existence of a heterocellular hereditary persistence of fetal hemoglobin (HPFH) determinant linked to beta thalassemia in a southern Italian population.
    Marinucci M, Mavilio F, Giuliani A, Gabbianelli M, Tentori L, Tentori L, Zorini CO, Lamberti E, Palazzolo A, Lanzo D.
    Hemoglobin; 1981 Jun; 5(1):1-17. PubMed ID: 6162827
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  • 7. 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; 22(3):205-12. PubMed ID: 2409283
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  • 8. 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; 29(1):137-48. PubMed ID: 1201197
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  • 10. 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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  • 11. Variations in globin synthesis in delta-beta-thalassaemia.
    Kinney TR, Friedman S, Cifuentes E, Kim HC, Schwartz E.
    Br J Haematol; 1978 Jan 15; 38(1):15-22. PubMed ID: 638060
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  • 20. The heterogeneity of normal Hb A2-beta thalassaemia in Greece.
    Kattamis C, Metaxotou-Mavromati A, Wood WG, Nash JR, Weatherall DJ.
    Br J Haematol; 1979 May 15; 42(1):109-23. PubMed ID: 465353
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