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Journal Abstract Search

320 related items for PubMed ID: 97892

  • 41. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
    Wong SC, Ali MA, Boyadjian SE.
    Acta Haematol; 1981; 65(3):157-63. PubMed ID: 6165216
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  • 42. Quantitation of Hb a2 with DE-52 microchromatography in whole blood as screening test for beta-thalassemia heterozygotes.
    Galanello R, Melis MA, Muroni P, Cao A.
    Acta Haematol; 1977; 57(1):32-6. PubMed ID: 402762
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  • 43. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
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  • 44. Deaths in beta-thalassemia/Hb E patients secondary to infections.
    Fucharoen S, Piankijagum A, Wasi P.
    Birth Defects Orig Artic Ser; 1987 Oct; 23(5A):495-500. PubMed ID: 3689937
    [No Abstract] [Full Text] [Related]

  • 45. Five families with homozygous delta-thalassaemia in Japan.
    Yasukawa M, Saito S, Fujita S, Ohta Y, Ikeda K, Matsumoto I, Kobayashi Y.
    Br J Haematol; 1980 Oct; 46(2):199-206. PubMed ID: 6158985
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  • 46. Comparison of haematological features of the beta0 and beta+ thalassaemia traits in Jamaican Negroes.
    Millard DP, Mason K, Serjeant BE, Serjeant GR.
    Br J Haematol; 1977 Jun; 36(2):161-70. PubMed ID: 871430
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  • 47. A study on the biochemical genetics of abnormal hemoglobins.
    I-Tao T.
    Sci Sin; 1975 Jun; 18(4):527-44. PubMed ID: 1202635
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  • 49. Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18).
    Sharma RS, Williams L, Wilson JB, Huisman TH.
    Biochim Biophys Acta; 1975 Jun 26; 393(2):379-82. PubMed ID: 1148221
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  • 50. Antibody response in beta-thalassemia/Hb E disease, hemoglobin H patients, and nonthalassemics with enteric fever.
    Rungpitarangsi B, Noytong S, Fucharoen S, Aswapokee N, Aswapokee P, Komolpit P, Tanphaichitr V, Rungpitarangsi V.
    Birth Defects Orig Artic Ser; 1987 Jun 26; 23(5A):527-33. PubMed ID: 3689942
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  • 54. [A2' (B2) hemoglobin associated with beta thalassemia and hereditary persistence of fetal hemoglobin. Study in 3 Colombian families].
    Echavarria A, Molina C, Zapata CI.
    Sangre (Barc); 1973 Jun 26; 18(2):145-56. PubMed ID: 4753554
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  • 55. Electrophoretic and chromatographic techniques for the differential diagnosis of a haemoglobin abnormality: Hb E heterozygosity.
    Bosisio AB, Rochette J, Wajcman H, Gianazza E, Righetti PG.
    J Chromatogr; 1985 Aug 23; 330(2):299-306. PubMed ID: 4066824
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  • 60. Study on nine families with haemoglobin Lepore in Campania: Hb Lepore trait, heterozygosity for Hb Lepore and beta-thalassaemia, homozygosity for Hb Lepore.
    Quattrin N, Bianchi P, Cimino R, De Rosa L, Dini E, Ventruto V.
    Acta Haematol; 1967 Aug 23; 37(5):266-75. PubMed ID: 4963514
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