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Journal Abstract Search

76 related items for PubMed ID: 1707848

  • 1. Deletion and non deletion hereditary persistence of fetal hemoglobin in Italy.
    Camaschella C, Serra A, Alfarano A, Gottardi E, Revello D, Bertero MT, Oggiano L, Longinotti M, Saglio G.
    Haematologica; 1990; 75 Suppl 5():26-30. PubMed ID: 1707848
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  • 4. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.
    Kalamaras A, Chassanidis C, Samara M, Papadakis MN, Vagena A, Aleporou-Marinou V, Patrinos GP, Kollia P.
    Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450
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  • 5. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL, Weatherall DJ.
    Prog Clin Biol Res; 1989 Sep; 316B():97-111. PubMed ID: 2482508
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  • 6. A conserved gene 3' to the HPFH-1 deletion breakpoint may have an effect on fetal globin gene expression in HPFH-1.
    Penny LA, Forget BG.
    Prog Clin Biol Res; 1989 Sep; 316B():133-41. PubMed ID: 2482494
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  • 9. Heterogeneity of molecular defects underlying hereditary persistence of fetal hemoglobin in Mediterranean area.
    Ottolenghi S, Giglioni B, Casini C, Merli S, Mantovani R, Comi P, Serra A, Guerrasio A, Camaschella C, Saglio G.
    Prog Clin Biol Res; 1985 Sep; 191():151-61. PubMed ID: 2413471
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  • 10. Mutations in the A gamma-globin promoter in hereditary persistence of fetal hemoglobin and delta beta zero-thalassemia.
    Ottolenghi S, Giglioni B, Comi P, Mantovani R, Malgaretti N, Nicolis S, Longinotti M, Sciarratta GV, Pirastu M, Camaschella C.
    Prog Clin Biol Res; 1987 Sep; 251():373-82. PubMed ID: 2448807
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  • 11. Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin.
    Tuan D, Murnane MJ, deRiel JL, Forget BG.
    Nature; 1980 May 29; 285(5763):335-7. PubMed ID: 6154897
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  • 12. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
    Feriotto G, Salvatori F, Finotti A, Breveglieri G, Venturi M, Zuccato C, Bianchi N, Borgatti M, Lampronti I, Mancini I, Massei F, Favre C, Gambari R.
    Acta Haematol; 2008 May 29; 119(1):28-37. PubMed ID: 18230963
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  • 13. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S, Fucharoen S, Surapot S, Fucharoen G, Sanchaisuriya K.
    Haematologica; 2004 Jul 29; 89(7):777-81. PubMed ID: 15257928
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  • 16. A tentative systematization of beta-thalassemia syndromes present in Northern Sardinia.
    Longinotti M, Masala B.
    Birth Defects Orig Artic Ser; 1982 Jul 29; 18(7):169-76. PubMed ID: 6186311
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  • 18. Support for the causal relationship between gamma globin gene promoter mutations and nondeletion forms of hereditary persistence of fetal hemoglobin.
    Metherall JE, Stoeckert CJ, Gillespie FP, Weissman SM, Forget BG.
    Prog Clin Biol Res; 1987 Jul 29; 251():347-61. PubMed ID: 2448805
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