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150 related items for PubMed ID: 3179447

  • 1. Molecular analysis of Japanese delta beta-thalassemia.
    Shiokawa S, Yamada H, Takihara Y, Matsunaga E, Ohba Y, Yamamoto K, Fukumaki Y.
    Blood; 1988 Nov; 72(5):1771-6. PubMed ID: 3179447
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  • 3. 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
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  • 4. 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 01; 6(2):226-37. PubMed ID: 2307466
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  • 6. 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 01; 72(2):636-41. PubMed ID: 2456798
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  • 7. A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
    Henthorn PS, Mager DL, Huisman TH, Smithies O.
    Proc Natl Acad Sci U S A; 1986 Jul 01; 83(14):5194-8. PubMed ID: 2425363
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  • 8. The 3' breakpoint of the yunnanese (Agammadeltabeta)0-thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the Ggamma-globin gene.
    Zhang XQ, Zhang JW.
    Hum Genet; 1998 Jul 01; 103(1):90-5. PubMed ID: 9737783
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  • 9. 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 01; 100(3-4):441-5. PubMed ID: 9272169
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  • 11. 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
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  • 13. 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 01; 71(2):457-62. PubMed ID: 2827815
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  • 14. 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
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  • 15. Laotian (delta beta) (0)-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobin.
    Zhang JW, Stamatoyannopoulos G, Anagnou NP.
    Blood; 1988 Sep 15; 72(3):983-8. PubMed ID: 2458154
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  • 16. 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 15; 68(4):971-4. PubMed ID: 2875756
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  • 17. 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
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  • 18. Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice.
    Anagnou NP, Perez-Stable C, Gelinas R, Costantini F, Liapaki K, Constantopoulou M, Kosteas T, Moschonas NK, Stamatoyannopoulos G.
    J Biol Chem; 1995 Apr 28; 270(17):10256-63. PubMed ID: 7537267
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  • 20. Structure of cloned delta-globin genes from a normal subject and a patient with delta-thalassemia; sequence polymorphisms found in the delta-globin gene region of Japanese individuals.
    Kimura A, Matsunaga E, Ohta Y, Fujiyoshi T, Matsuo T, Nakamura T, Imamura T, Yanase T, Takagi Y.
    Nucleic Acids Res; 1982 Oct 11; 10(19):5725-32. PubMed ID: 6292847
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