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Journal Abstract Search

140 related items for PubMed ID: 1689188

  • 1. 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
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  • 3. 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 15; 79(7):2347-51. PubMed ID: 6179097
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  • 5. 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 15; 100(3-4):441-5. PubMed ID: 9272169
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  • 6. Molecular characterisation of Vietnamese HPFH.
    Motum PI, Hamilton TJ, Lindeman R, Le H, Trent RJ.
    Hum Mutat; 1993 Sep 15; 2(3):179-84. PubMed ID: 7689901
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  • 7. 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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  • 12. Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.
    Elder JT, Forrester WC, Thompson C, Mager D, Henthorn P, Peretz M, Papayannopoulou T, Groudine M.
    Mol Cell Biol; 1990 Apr 15; 10(4):1382-9. PubMed ID: 1690839
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  • 15. High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.
    Arcasoy MO, Romana M, Fabry ME, Skarpidi E, Nagel RL, Forget BG.
    Mol Cell Biol; 1997 Apr 15; 17(4):2076-89. PubMed ID: 9121456
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  • 19. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
    Bollekens JA, Forget BG.
    Hematol Oncol Clin North Am; 1991 Jun 15; 5(3):399-422. PubMed ID: 1713909
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  • 20. 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
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