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Journal Abstract Search

142 related items for PubMed ID: 2409869

  • 21. 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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  • 23. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
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  • 25. Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
    Carrocini GC, Ondei LS, Zamaro PJ, Bonini-Domingos CR.
    Genet Mol Res; 2011 Dec 21; 10(4):3213-9. PubMed ID: 22194178
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  • 26. One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.
    Efremov GD, Gjorgovski I, Stojanovski N, Diaz-Chico JC, Harano T, Kutlar F, Huisman TH.
    Hum Genet; 1987 Oct 21; 77(2):132-6. PubMed ID: 2443439
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  • 29. 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 21; 21(4):263-7. PubMed ID: 6208362
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  • 32. Multiple mutations produce delta beta 0 thalassemia in Sardinia.
    Pirastu M, Kan YW, Galanello R, Cao A.
    Science; 1984 Mar 02; 223(4639):929-30. PubMed ID: 6198720
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  • 33. A patient of German descent with (delta beta)0-thalassemia carrying the Sicilian type deletion of the delta and beta globin genes.
    Hopmeier P, Shenhav A, Glaser G, Rachmilewitz EA, Oppenheim A.
    Hemoglobin; 1988 Mar 02; 12(1):39-51. PubMed ID: 3384697
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  • 34. Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin.
    Old JM, Ayyub H, Wood WG, Clegg JB, Weatherall DJ.
    Science; 1982 Feb 19; 215(4535):981-2. PubMed ID: 6186021
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  • 40. 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 19; 70(2):593-6. PubMed ID: 2440503
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