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Journal Abstract Search

130 related items for PubMed ID: 1715793

  • 1.
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  • 2. Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.
    Hatton CS, Wilkie AO, Drysdale HC, Wood WG, Vickers MA, Sharpe J, Ayyub H, Pretorius IM, Buckle VJ, Higgs DR.
    Blood; 1990 Jul 01; 76(1):221-7. PubMed ID: 2364173
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  • 3. (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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  • 6. The proximal element of the beta globin locus control region is not functionally required in vivo.
    Kulozik AE, Bail S, Bellan-Koch A, Bartram CR, Kohne E, Kleihauer E.
    J Clin Invest; 1991 Jun 15; 87(6):2142-6. PubMed ID: 2040696
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  • 7. The inactive beta globin gene on a gamma delta beta thalassemia chromosome has a normal structure and functions normally in vitro.
    Curtin PT, Kan YW.
    Blood; 1988 Mar 15; 71(3):766-70. PubMed ID: 3345345
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  • 8. Embryonic zeta-globin chains in adults: a marker for alpha-thalassemia-1 haplotype due to a greater than 17.5-kb deletion.
    Chui DH, Wong SC, Chung SW, Patterson M, Bhargava S, Poon MC.
    N Engl J Med; 1986 Jan 09; 314(2):76-9. PubMed ID: 3941693
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  • 9. Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites.
    Driscoll MC, Dobkin CS, Alter BP.
    Proc Natl Acad Sci U S A; 1989 Oct 09; 86(19):7470-4. PubMed ID: 2798417
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  • 10. Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion.
    Anand R, Boehm CD, Kazazian HH, Vanin EF.
    Blood; 1988 Aug 09; 72(2):636-41. PubMed ID: 2456798
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  • 11. Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families.
    Griese EU, Kohne E, Horst J.
    Hum Genet; 1985 Aug 09; 71(2):134-7. PubMed ID: 2995233
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  • 12. High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region.
    Waye JS, Cai SP, Eng B, Clark C, Adams JG, Chui DH, Steinberg MH.
    Blood; 1991 Mar 01; 77(5):1100-3. PubMed ID: 1995096
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  • 13. Interaction of heterozygous beta (0)-thalassemia and triplicated alpha globin loci in a Swiss-Spanish family.
    Beris P, Darbellay R, Hochmann A, Pradervand E, Pugin P.
    Klin Wochenschr; 1991 Oct 02; 69(15):710-4. PubMed ID: 1795494
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  • 14. The molecular basis of alpha thalassaemia in a South African population.
    Mathew CG, Rousseau J, Rees JS, Harley EH.
    Br J Haematol; 1983 Sep 02; 55(1):103-11. PubMed ID: 6309210
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  • 15. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Sep 02; 82(3):269-80. PubMed ID: 9234571
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  • 16. Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
    Embury SH, Miller JA, Dozy AM, Kan YW, Chan V, Todd D.
    J Clin Invest; 1980 Dec 02; 66(6):1319-25. PubMed ID: 7440717
    [Abstract] [Full Text] [Related]

  • 17. The Corfu delta beta zero thalassemia: a small deletion acts at a distance to selectively abolish beta globin gene expression.
    Kulozik AE, Yarwood N, Jones RW.
    Blood; 1988 Feb 02; 71(2):457-62. PubMed ID: 2827815
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  • 18. The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes.
    Efremov GD, Nikolov N, Hattori Y, Bakioglu I, Huisman TH.
    Blood; 1986 Oct 02; 68(4):971-4. PubMed ID: 2875756
    [Abstract] [Full Text] [Related]

  • 19. Compensatory increase in alpha 1-globin gene expression in individuals heterozygous for the alpha-thalassemia-2 deletion.
    Liebhaber SA, Cash FE, Main DM.
    J Clin Invest; 1985 Sep 02; 76(3):1057-64. PubMed ID: 4044827
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  • 20. Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.
    Sanguansermsri T, Pape M, Laig M, Hundrieser J, Flatz G.
    Hemoglobin; 1990 Sep 02; 14(2):157-68. PubMed ID: 2272839
    [Abstract] [Full Text] [Related]

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