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Journal Abstract Search

150 related items for PubMed ID: 6163196

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  • 23. Variations in globin chain synthesis in hereditary persistence of fetal haemoglobin.
    Friedman S, Schwartz E, Ahern E, Ahern V.
    Br J Haematol; 1976 Mar; 32(3):357-64. PubMed ID: 1252370
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  • 26. Balanced globin chain synthesis in hereditary persistence of fetal hemoglobin.
    Natta CL, Niazi GA, Ford S, Bank A.
    J Clin Invest; 1974 Aug; 54(2):433-8. PubMed ID: 4847253
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  • 28. Heterogeneity of beta thalassaemia in Thailand.
    Yenchitsomanus P, Baramee A, Fucharoen S, Pootrakul P, Wasi P.
    Southeast Asian J Trop Med Public Health; 1982 Dec; 13(4):618-27. PubMed ID: 6189197
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  • 29. Greek (A gamma) variant of hereditary persistence of fetal haemoglobin: globin gene organization and studies of expression of fetal haemoglobins in clonal erythroid cultures.
    Papayannopoulou T, Lawn RM, Stamatoyannopoulos G, Maniatis T.
    Br J Haematol; 1982 Mar; 50(3):387-99. PubMed ID: 6175332
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  • 33. Beta-thalassaemia-87 C-->G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients.
    De Angioletti M, Lacerra G, Pagano L, Alessi M, D'Avino R, Manca L, Carestia C.
    Br J Haematol; 2004 Sep; 126(5):743-9. PubMed ID: 15327529
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  • 36. Intrinsic potential for high fetal hemoglobin production in a Druz family with beta-thalassemia is due to an unlinked genetic determinant.
    Oppenheim A, Yaari A, Rund D, Rachmilewitz EA, Nathan D, Wong C, Kazazian HH, Miller B.
    Hum Genet; 1990 Dec; 86(2):175-80. PubMed ID: 1702403
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  • 37. G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C.
    Higgs DR, Clegg JB, Wood WG, Weatherall DJ.
    J Med Genet; 1979 Aug; 16(4):288-95. PubMed ID: 490582
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