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Journal Abstract Search

118 related items for PubMed ID: 444685

  • 1.
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  • 2. Globin chain synthesis in beta-thalassemia with normal hemoglobins A2 and F.
    Aksoy M, Almiş G, Bermek E.
    Hemoglobin; 1979; 3(4):263-70. PubMed ID: 500371
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  • 3. Cord blood study on beta-thalassemia and hemoglobin E.
    Pootrakul S, Muang-sup V, Fucharoen S, Wasi P.
    Am J Med Genet; 1988 Jan; 29(1):49-57. PubMed ID: 2449818
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  • 5. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
    Haji F, Chadli A, Fattoum S, Souilem J, Hassine L.
    Arch Inst Pasteur Tunis; 1985 Dec; 62(4):341-53. PubMed ID: 2423045
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  • 11. 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; 42(1):109-23. PubMed ID: 465353
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  • 13. Homozygous delta thalassemia in Japan.
    Ohta Y, Yasukawa M, Saito S, Fujita S, Kobayashi Y.
    Hemoglobin; 1980 May; 4(3-4):417-25. PubMed ID: 6158498
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  • 15. Double heterozygosis for hemoglobin C-beta thalassemia: description of a Spanish family. Hemoglobin C-beta thalassemia in a Spanish family.
    Casado A, Pellicer A, Olmeda F, Hors P, Gonzalez-Sotos MA, Carmona MS, Lopez-Fernandez ME.
    Clin Genet; 1978 Mar; 13(3):265-70. PubMed ID: 639336
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  • 16. The quiet carrier of beta-thalassemia.
    Kelleher JF, Schwartz E.
    Am J Pediatr Hematol Oncol; 1979 Mar; 1(1):15-7. PubMed ID: 543507
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  • 17. The interaction of alpha-thalassemia and homozygous sickle-cell disease.
    Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR.
    N Engl J Med; 1982 Jun 17; 306(24):1441-6. PubMed ID: 6176865
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  • 18. A Family with γ-Thalassemia and High Hb A2 Levels.
    Parmeggiani G, Gualandi F, Selvatici R, Rimessi P, Bigoni S, Taddei Masieri M, Dolcini B, Venturoli A, Cappabianca MP, Ferlini A, Ravani A.
    Hemoglobin; 2016 Jun 17; 40(3):187-90. PubMed ID: 27117568
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  • 19. 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 Jun 17; 66(2-3):151-6. PubMed ID: 6201431
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  • 20. [Intermediate thalassemia. Study of 5 cases in their clinical, ferrokinetic and erythrokinetic aspects].
    Muñoz JA, Martín MV, Risueño CE, Freire J, Pajares M, Campos J.
    Sangre (Barc); 1989 Oct 17; 34(5):346-9. PubMed ID: 2482545
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