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Journal Abstract Search

370 related items for PubMed ID: 5438669

  • 1. [Heterozygous beta-thalassemia without icrease of hemoglobin A2].
    Marti HR, Grieder HR.
    Schweiz Med Wochenschr; 1970 Apr 11; 100(15):663-6. PubMed ID: 5438669
    [No Abstract] [Full Text] [Related]

  • 2. [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 Apr 11; 18(2):145-56. PubMed ID: 4753554
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  • 3. [Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].
    Haji F, Chadli A, Fattoum S, Souilem J, Hassine L.
    Arch Inst Pasteur Tunis; 1985 Dec 11; 62(4):341-53. PubMed ID: 2423045
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  • 4. [Genetic and hematological study of a family from Ghana suffering from hereditary persistence of fetal hemoglobin associated with beta-thalassemia and hemoglobinosis S].
    Boreux G, Wyss M, Farquet JJ.
    Arch Genet (Zur); 1973 Dec 11; 46(1):22-33. PubMed ID: 4731929
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  • 10. Inclusion-body beta-thalassemia trait. A form of beta thalassemia producing clinical manifestations in simple heterozygotes.
    Stamatoyannopoulos G, Woodson R, Papayannopoulou T, Heywood D, Kurachi S.
    N Engl J Med; 1974 Apr 25; 290(17):939-43. PubMed ID: 4361439
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  • 13. First association in Spain of Hb J Baltimore alpha A2 beta 2 16 (A13) Gly replaced by Asp and beta o thalassemia.
    Romero C, Muñoz A, Fernández Fuertes I, Hernández-Jodra M, Navarro JL.
    Hemoglobin; 1982 Apr 25; 6(6):607-12. PubMed ID: 7161107
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  • 15. [Double heterozygous predisposition for Hb P ( 2 2 117 His--Arg ) and the classic -thalassemia in an Aargau-family].
    Rosenmund A, Winterhalter KH, Haber J, Marti HR.
    Schweiz Med Wochenschr; 1972 Nov 04; 102(44):1624-6. PubMed ID: 4645055
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  • 16. Haemoglobin E-beta-thalassaemia; a study of eight cases in Northwest India.
    Ghosh K, Chakrabarty AK, Mohanty D, Das KC.
    Trop Geogr Med; 1983 Sep 04; 35(3):267-71. PubMed ID: 6196886
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