These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

126 related items for PubMed ID: 2440503

  • 1. The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases.
    Camaschella C, Serra A, Saglio G, Baiget M, Malgaretti N, Mantovani R, Ottolenghi S.
    Blood; 1987 Aug; 70(2):593-6. PubMed ID: 2440503
    [Abstract] [Full Text] [Related]

  • 2. Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the beta-globin gene cluster.
    Kosteas T, Palena A, Anagnou NP.
    Hum Genet; 1997 Sep; 100(3-4):441-5. PubMed ID: 9272169
    [Abstract] [Full Text] [Related]

  • 3. Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.
    Tuan D, Feingold E, Newman M, Weissman SM, Forget BG.
    Proc Natl Acad Sci U S A; 1983 Nov; 80(22):6937-41. PubMed ID: 6196781
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Italian type of deletional hereditary persistence of fetal hemoglobin.
    Saglio G, Camaschella C, Serra A, Bertero T, Rege Cambrin G, Guerrasio A, Mazza U, Izzo P, Terragni F, Giglioni B.
    Blood; 1986 Sep; 68(3):646-51. PubMed ID: 2427137
    [Abstract] [Full Text] [Related]

  • 6. The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases.
    Collins FS, Cole JL, Lockwood WK, Iannuzzi MC.
    Blood; 1987 Dec; 70(6):1797-803. PubMed ID: 2445400
    [Abstract] [Full Text] [Related]

  • 7. Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
    Vives-Corrons JL, Pujades MA, Miguel-García A, Miguel-Sosa A, Cambiazzo S.
    Blood; 1992 Sep 15; 80(6):1582-5. PubMed ID: 1520881
    [Abstract] [Full Text] [Related]

  • 8. A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer.
    Camaschella C, Serra A, Gottardi E, Alfarano A, Revello D, Mazza U, Saglio G.
    Blood; 1990 Feb 15; 75(4):1000-5. PubMed ID: 1689188
    [Abstract] [Full Text] [Related]

  • 9. Molecular characterization of a novel form of (A gamma delta beta)zero-thalassemia deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism.
    Anagnou NP, Papayannopoulou T, Nienhuis AW, Stamatoyannopoulos G.
    Nucleic Acids Res; 1988 Jul 11; 16(13):6057-66. PubMed ID: 2456521
    [Abstract] [Full Text] [Related]

  • 10. Eastern European (delta beta) zero-thalassemia: molecular characterization of a novel 9.1-kb deletion resulting in high levels of fetal hemoglobin in the adult.
    Palena A, Blau A, Stamatoyannopoulos G, Anagnou NP.
    Blood; 1994 Jun 15; 83(12):3738-45. PubMed ID: 7515720
    [Abstract] [Full Text] [Related]

  • 11. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification.
    Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL.
    Blood; 1994 Mar 15; 83(6):1673-82. PubMed ID: 7510147
    [Abstract] [Full Text] [Related]

  • 12. Molecular characterization and PCR detection of a deletional HPFH: application to rapid prenatal diagnosis for compound heterozygotes of this defect with beta-thalassemia in a Chinese family.
    Xu XM, Li ZQ, Liu ZY, Zhong XL, Zhao YZ, Mo QH.
    Am J Hematol; 2000 Nov 15; 65(3):183-8. PubMed ID: 11074532
    [Abstract] [Full Text] [Related]

  • 13. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.
    Losekoot M, Fodde R, Gerritsen EJ, van de Kuit I, Schreuder A, Giordano PC, Vossen JM, Bernini LF.
    Blood; 1991 Feb 15; 77(4):861-7. PubMed ID: 1704267
    [Abstract] [Full Text] [Related]

  • 14. Nucleotide sequence of the Belgian G gamma+(A gamma delta beta)0-thalassemia deletion breakpoint suggests a common mechanism for a number of such recombination events.
    Fodde R, Losekoot M, Casula L, Bernini LF.
    Genomics; 1990 Dec 15; 8(4):732-5. PubMed ID: 2276746
    [Abstract] [Full Text] [Related]

  • 15. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
    Feingold EA, Forget BG.
    Blood; 1989 Nov 01; 74(6):2178-86. PubMed ID: 2478223
    [Abstract] [Full Text] [Related]

  • 16. A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints.
    Mager DL, Henthorn PS, Smithies O.
    Nucleic Acids Res; 1985 Sep 25; 13(18):6559-75. PubMed ID: 2997715
    [Abstract] [Full Text] [Related]

  • 17. Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpoints.
    Henthorn PS, Smithies O, Mager DL.
    Genomics; 1990 Feb 25; 6(2):226-37. PubMed ID: 2307466
    [Abstract] [Full Text] [Related]

  • 18. The deletion in a type of delta 0-beta 0-thalassaemia begins in an inverted AluI repeat.
    Ottolenghi S, Giglioni B.
    Nature; 1982 Dec 23; 300(5894):770-1. PubMed ID: 6184621
    [Abstract] [Full Text] [Related]

  • 19. A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia.
    Giglioni B, Casini C, Mantovani R, Merli S, Comi P, Ottolenghi S, Saglio G, Camaschella C, Mazza U.
    EMBO J; 1984 Nov 23; 3(11):2641-5. PubMed ID: 6210198
    [Abstract] [Full Text] [Related]

  • 20. A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia.
    Kulozik AE, Bellan-Koch A, Kohne E, Kleihauer E.
    Blood; 1992 May 01; 79(9):2455-9. PubMed ID: 1571556
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.