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Journal Abstract Search

142 related items for PubMed ID: 2409869

  • 1. Heterogeneity of delta, beta-thalassemia and hereditary persistence of Hb F in the Mediterranean area.
    Ottolenghi S, Giglioni B, Comi P, Guida S, Casini C, Merli S, Mantovani R, Terragni F, Aghib D, Saglio G.
    Ann N Y Acad Sci; 1985; 445():170-6. PubMed ID: 2409869
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  • 2. 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; 79(7):2347-51. PubMed ID: 6179097
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  • 3. Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin.
    Tuan D, Murnane MJ, deRiel JL, Forget BG.
    Nature; 1980 May 29; 285(5763):335-7. PubMed ID: 6154897
    [No Abstract] [Full Text] [Related]

  • 4. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
    Bollekens JA, Forget BG.
    Hematol Oncol Clin North Am; 1991 Jun 29; 5(3):399-422. PubMed ID: 1713909
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  • 12. Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.
    Oner C, Gurgey A, Altay C, Kutlar F, Huisman TH.
    Am J Hematol; 1990 Jul 29; 34(3):230-1. PubMed ID: 1694630
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  • 14. Analysis of globin gene structure in patients with beta thalassemia by restriction endonuclease mapping.
    Tam JW, Kaufman RE, Nienhuis AW.
    Hemoglobin; 1981 Jul 29; 5(3):209-15. PubMed ID: 6164667
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  • 15. Hemoglobin F in beta thalassemia and related conditions.
    Schroeder WA, Huisman TH.
    Ann N Y Acad Sci; 1980 Jul 29; 344():240-52. PubMed ID: 6156626
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  • 17. (delta beta) zero thalassemia of the Southern Italian type. Its geographical origin and interaction with the sickle cell gene.
    Trent RJ, Svirklys L, Harris MG, Hocking DR, Kronenberg H.
    Pathology; 1986 Jan 29; 18(1):117-22. PubMed ID: 2425331
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  • 19. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R, Podda A, Melis MA, Monne M, Cao A.
    Prog Clin Biol Res; 1989 Jan 29; 316B():113-21. PubMed ID: 2482492
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