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126 related items for PubMed ID: 6171165

  • 1. Two siblings with unusually mild homozygous beta-thalassemia: a didactic example of the effect of a nonallelic modifier gene of the expressivity of a monogenic disorder.
    Prchal J, Stamatoyannopoulos G.
    Am J Med Genet; 1981; 10(3):291-300. PubMed ID: 6171165
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  • 4. Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinism.
    Schilirò G, Pavone L, Romeo MA, Russo A, Musumeci S, Russo G.
    Am J Med Genet; 1983 Jun; 15(2):225-31. PubMed ID: 6192718
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  • 14. Beta-thalassemia with exceptionally high hemoglobin A2. Differential expression of the delta-globin gene in the presence of beta-thalassemia.
    Steinberg MH, Coleman MB, Adams JG.
    J Lab Clin Med; 1982 Oct; 100(4):548-57. PubMed ID: 6288819
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  • 16. [The molecular basis of hereditary persistence of fetal hemoglobin (HPFH). Clinical importance of the hemoglobin switching mechanism with special reference to Corfu delta beta zero thalassemia].
    Kulozik AE, Kohne E, Kleihauer E.
    Monatsschr Kinderheilkd; 1988 Nov; 136(11):751-7. PubMed ID: 2464759
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  • 17. Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.
    Thein SL, Sampietro M, Rohde K, Rochette J, Weatherall DJ, Lathrop GM, Demenais F.
    Am J Hum Genet; 1994 Feb; 54(2):214-28. PubMed ID: 7508182
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  • 18. Biosynthetic studies and gamma-chain composition in the Greek type of hereditary persistence of fetal hemoglobin and in its association with beta-thalassemia.
    Camaschella C, Ciocca-Vasino MA, Guerrasio A, Balegno G, Barberis E, Delponte D, Saglio G.
    Acta Haematol; 1979 Feb; 61(5):272-7. PubMed ID: 111454
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  • 20. Asymptomatic homozygous deletional beta(0)-thalassemia in an African individual.
    Faustino P, Reis AB, Feliciano H, Ferrão L, Pereira P, Picanço I, Miranda A, Seixas T, Romão L, Júnior EC, Lavinha J.
    Am J Hematol; 2002 Jul; 70(3):232-6. PubMed ID: 12111769
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