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Journal Abstract Search

174 related items for PubMed ID: 2423109

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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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  • 4. Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese families.
    Zeng YT, Huang SZ, Chen B, Liang YC, Chang ZM, Harano T, Huisman TH.
    Blood; 1985 Dec; 66(6):1430-5. PubMed ID: 2415188
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  • 8. Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia.
    Clegg JB, Metaxatou-Mavromati A, Kattamis C, Sofroniadou K, Wood WG, Weatherall DJ.
    Br J Haematol; 1979 Dec; 43(4):521-36. PubMed ID: 93488
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  • 9. 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
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  • 10. Delta Beta-Thalassaemia in two yugoslavian families.
    Efremov GD, Nikolov N, Duma H, Schroeder WA, Miller A, Huisman TH.
    Scand J Haematol; 1975 May 15; 14(3):226-32. PubMed ID: 1145125
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  • 11. 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
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  • 12. Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand.
    Trachoo O, Sura T, Sakuntabhai A, Singhasivanon P, Krudsood S, Phimpraphi W, Krasaesub S, Chanjarunee S, Looareesuwan S.
    Hemoglobin; 2003 May 23; 27(2):97-104. PubMed ID: 12779271
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  • 14. Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.
    Cianetti L, Care A, Sposi NM, Giampaolo A, Calandrini M, Petrini M, Massa A, Marinucci M, Mavilio F, Ceccanti M.
    J Med Genet; 1984 Aug 23; 21(4):263-7. PubMed ID: 6208362
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  • 15. Molecular characterization of a novel form of (A gamma delta beta)zero thalassemia deletion in a Chinese family.
    Zhang JW, Song WF, Zhao YJ, Wu GY, Qiu ZM, Wang FN, Chen SS, Stamatoyannopoulos G.
    Blood; 1993 Mar 15; 81(6):1624-9. PubMed ID: 7680922
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  • 17. Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.
    Sofroniadou K, Wood WG, Nute PE, Stamatoyannopoulos G.
    Br J Haematol; 1975 Jan 15; 29(1):137-48. PubMed ID: 1201197
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  • 18. Greek (A gamma) variant of hereditary persistence of fetal haemoglobin: globin gene organization and studies of expression of fetal haemoglobins in clonal erythroid cultures.
    Papayannopoulou T, Lawn RM, Stamatoyannopoulos G, Maniatis T.
    Br J Haematol; 1982 Mar 15; 50(3):387-99. PubMed ID: 6175332
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  • 19. Association of thalassaemia intermedia with a beta-globin gene haplotype.
    Thein SL, Wainscoat JS, Sampietro M, Old JM, Cappellini D, Fiorelli G, Modell B, Weatherall DJ.
    Br J Haematol; 1987 Mar 15; 65(3):367-73. PubMed ID: 2436649
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