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Journal Abstract Search


197 related items for PubMed ID: 13899597

  • 1. [Thalassemia and abnormal hemoglobins in the Aegean region of Anatolia].
    GOKSEL V, TARTAROGLU N.
    Rev Med Moyen Orient; 1962; 19():58-64. PubMed ID: 13899597
    [No Abstract] [Full Text] [Related]

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  • 3. A family with S and C hemoglobins and the hereditary persistence of F hemoglobin. A comparison of C thalassemia disease with the CF syndrome.
    SCHNEIDER RG, LEVIN WC, EVERETT C.
    N Engl J Med; 1961 Dec 28; 265():1278-83. PubMed ID: 13908956
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  • 5. Studies on abnormal hemoglobins. X. A new syndrome: hemoglobin C-thalassemia disease.
    SINGER K, KRAUS AP, SINGER L, RUBINSTEIN HM, GOLDBERG SR.
    Blood; 1954 Nov 28; 9(11):1032-46. PubMed ID: 13208755
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  • 7. Homozygous Lepore haemoglobin disease appearing as thalassaemia major in two Papuan siblings.
    NEEB H, BEIBOER JL, JONXIS JH, KAARS SIJPESTEIJN JA, MULLER CJ.
    Trop Geogr Med; 1961 Sep 28; 13():207-15. PubMed ID: 14478740
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  • 10. [Microcytosis and hemoglobin a.r. in the genetics of thalassemia].
    ROMEO G.
    Boll Soc Ital Biol Sper; 1960 Mar 15; 36():219-21. PubMed ID: 14438611
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  • 12. Hemoglobin "pylos": study of a hemoglobinopathy resembling thalassemia in the heterozygous, homozygous and double heterozygous state.
    FESSAS P, STAMATOYANNOPOULOS G, KARAKLIS A.
    Blood; 1962 Jan 15; 19():1-22. PubMed ID: 13892631
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  • 14. Some remarks on hemoglobinopathies with particular reference to thalassemia.
    JONXIS JH.
    J Pediatr; 1961 Nov 15; 59():765-76. PubMed ID: 14452400
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  • 15. Thalassemia-hemoglobin C disease; a new syndrome presumably due to the combination of the genes for thalassemia and hemoglobin C.
    ZUELZER WW, KAPLAN E.
    Blood; 1954 Nov 15; 9(11):1047-54. PubMed ID: 13208756
    [No Abstract] [Full Text] [Related]

  • 16. [On the behavior of different types of hemoglobin (Hb A, A2, F, S and "Bart's") in thalassemia, drepanocytosis and microdrepanocythemia].
    VENTRUTO V, DE ROSA L, CIMINO R, QUATTRIN N.
    Schweiz Med Wochenschr; 1962 Oct 20; 92():1322-4. PubMed ID: 13996677
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  • 17. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 20; 82(1):1-5. PubMed ID: 13230906
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  • 18. Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis.
    SINGER K, SINGER L, GOLDBERG SR.
    Blood; 1955 May 20; 10(5):405-15. PubMed ID: 14363321
    [No Abstract] [Full Text] [Related]

  • 19. Inclusions of hemoglobin erythroblasts and erythrocytes of thalassemia.
    FESSAS P.
    Blood; 1963 Jan 20; 21():21-32. PubMed ID: 13944958
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  • 20. Sickle cell haemoglobin and two types of thalassaemia in the same family.
    RUSSO G, MOLLICA F.
    Acta Haematol; 1962 Jan 20; 28():329-40. PubMed ID: 13975667
    [No Abstract] [Full Text] [Related]


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