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Journal Abstract Search

118 related items for PubMed ID: 3209408

  • 21. Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype.
    Waye JS, Chui DH, Eng B, Cai SP, Coleman MB, Adams JG, Steinberg MH.
    Am J Hematol; 1991 Oct; 38(2):108-12. PubMed ID: 1719807
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  • 22. Comparative approach to the evaluation of hemoglobin A2 by two different methods: high-performance liquid chromatography and DE-52 microchromatography.
    Samperi P, Testa R, Mancuso M, Schilirò G.
    Acta Haematol; 1990 Oct; 83(4):179-82. PubMed ID: 2115713
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  • 25. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R, Podda A, Melis MA, Monne M, Cao A.
    Prog Clin Biol Res; 1989 Oct; 316B():113-21. PubMed ID: 2482492
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  • 27. Quantitation of hemoglobin A2 in alpha thalassemia trait by microcolumn chromatography.
    McCormack MK.
    Clin Chim Acta; 1980 Aug 19; 105(3):387-91. PubMed ID: 7408198
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  • 28.
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  • 29. Evaluation of a commercial kit for microchromatographic quantitation of hemoglobin A2 in the presence of hemoglobin S.
    Baine RM, Brown HG.
    Clin Chem; 1981 Jul 19; 27(7):1244-7. PubMed ID: 7237791
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  • 30. Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.
    Schroeder WA, Powars DR, Kay LM, Chan LS, Huynh V, Shelton JB, Shelton JR.
    Hemoglobin; 1989 Jul 19; 13(4):325-53. PubMed ID: 2473969
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  • 31.
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  • 32. Evaluation of a simplified microchromatographic technique for hemoglobin A2 determination.
    Moors A, Melis-Liekens J, De Vlieger-Bensel M, De Groof-Cornelis E, Van Ros G.
    Acta Haematol; 1979 Jul 19; 61(1):15-26. PubMed ID: 105535
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  • 33.
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  • 34. Hemoglobin A2: origin, evolution, and aftermath.
    Steinberg MH, Adams JG.
    Blood; 1991 Nov 01; 78(9):2165-77. PubMed ID: 1932737
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  • 35. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.
    Giampaolo A, Mavilio F, Sposi NM, Carè A, Massa A, Cianetti L, Petrini M, Russo R, Cappellini MD, Marinucci M.
    Hum Genet; 1984 Nov 01; 66(2-3):151-6. PubMed ID: 6201431
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  • 36. Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.
    Oggiano L, Pirastu M, Moi P, Longinotti M, Perseu L, Cao A.
    Br J Haematol; 1987 Oct 01; 67(2):225-9. PubMed ID: 3676110
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  • 37.
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  • 38. Diagnostic efficacy of haemoglobin A2 in heterozygous beta thalassaemia.
    Saraya AK, Kumar R, Choudhry VP, Tyagi RS, Sehgal AK.
    Indian J Med Res; 1984 Aug 01; 80():203-8. PubMed ID: 6210250
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  • 39.
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  • 40. Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction.
    Melis MA, Pirastu M, Galanello R, Furbetta M, Tuveri T, Cao A.
    Blood; 1983 Jul 01; 62(1):226-9. PubMed ID: 6305442
    [Abstract] [Full Text] [Related]

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