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Journal Abstract Search

165 related items for PubMed ID: 2986746

  • 1. Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.
    Nicholls RD, Higgs DR, Clegg JB, Weatherall DJ.
    Blood; 1985 Jun; 65(6):1434-8. PubMed ID: 2986746
    [Abstract] [Full Text] [Related]

  • 2. Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
    Pressley L, Higgs DR, Clegg JB, Weatherall DJ.
    Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3586-9. PubMed ID: 6158051
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  • 3. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
    Lie-Injo LE, Herrera AR, Lebo RV, Hassan K, Lopez CG.
    Am J Hematol; 1985 Mar; 18(3):289-96. PubMed ID: 2983536
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  • 4. Hb Bart's level in cord blood and deletions of alpha-globin genes.
    Lie-Injo LE, Solai A, Herrera AR, Nicolaisen L, Kan YW, Wan WP, Hasan K.
    Blood; 1982 Feb; 59(2):370-6. PubMed ID: 6895707
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  • 5. Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.
    Galanello R, Melis MA, Maccioni L, Pirastu M, Cao A.
    Pediatr Res; 1984 Feb; 18(2):158-62. PubMed ID: 6322098
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  • 6. Molecular basis of hemoglobin-H disease in the Mediterranean population.
    Kan YW, Dozy AM, Stamatoyannopoulos G, Hadjiminas MG, Zachariades Z, Furbetta M, Cao A.
    Blood; 1979 Dec; 54(6):1434-8. PubMed ID: 508946
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  • 7. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
    Bowden DK, Hill AV, Higgs DR, Oppenheimer SJ, Weatherall DJ, Clegg JB.
    J Clin Invest; 1987 Jan; 79(1):39-43. PubMed ID: 3793931
    [Abstract] [Full Text] [Related]

  • 8. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
    Steinberg MH, Coleman MB, Adams JG, Hartmann RC, Saba H, Anagnou NP.
    Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
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  • 12. Identification of a nondeletion defect in alpha-thalassemia.
    Kan YW, Dozy AM, Trecartin R, Todd D.
    N Engl J Med; 1977 Nov 17; 297(20):1081-4. PubMed ID: 909565
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  • 14. (Alpha)alpha 5.3: a novel alpha(+)-thalassemia deletion with the breakpoints in the alpha 2-globin gene and in close proximity to an Alu family repeat between the psi alpha 2- and psi alpha 1-globin genes.
    Lacerra G, Fioretti G, De Angioletti M, Pagano L, Guarino E, de Bonis C, Viola A, Maglione G, Scarallo A, De Rosa L.
    Blood; 1991 Nov 15; 78(10):2740-6. PubMed ID: 1824266
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  • 15. The molecular basis of alpha thalassaemia in a South African population.
    Mathew CG, Rousseau J, Rees JS, Harley EH.
    Br J Haematol; 1983 Sep 15; 55(1):103-11. PubMed ID: 6309210
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  • 16. Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
    Embury SH, Lebo RV, Dozy AM, Kan YW.
    J Clin Invest; 1979 Jun 15; 63(6):1307-10. PubMed ID: 447845
    [Abstract] [Full Text] [Related]

  • 17. The molecular basis of alpha-thalassaemia in Thailand.
    Winichagoon P, Higgs DR, Goodbourn SE, Clegg JB, Weatherall DJ, Wasi P.
    EMBO J; 1984 Aug 15; 3(8):1813-8. PubMed ID: 6548185
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  • 20. Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families.
    Griese EU, Kohne E, Horst J.
    Hum Genet; 1985 Aug 15; 71(2):134-7. PubMed ID: 2995233
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