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Journal Abstract Search

318 related items for PubMed ID: 13908956

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. [On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"].
    MANGANELLI G, DALFINO G, TANNOIA N.
    Haematologica; 1962 Dec 28; 47():353-66. PubMed ID: 14469260
    [No Abstract] [Full Text] [Related]

  • 3. [Some hereditary blood disorders].
    TETRY A.
    Biol Med (Paris); 1953 Jul 28; 42(4):317-27. PubMed ID: 13081682
    [No Abstract] [Full Text] [Related]

  • 4. Studies on abnormal hemoglobins. XIII. Hemoglobin S-thalassemia disease and hemoglobin C-thalassemia disease in siblings.
    SINGER K, JOSEPHSON AM, SINGER L, HELLER P, ZIMMERMAN HJ.
    Blood; 1957 Jul 28; 12(7):593-602. PubMed ID: 13436515
    [No Abstract] [Full Text] [Related]

  • 5. [Thalassemia and abnormal hemoglobins in the Aegean region of Anatolia].
    GOKSEL V, TARTAROGLU N.
    Rev Med Moyen Orient; 1962 Jul 28; 19():58-64. PubMed ID: 13899597
    [No Abstract] [Full Text] [Related]

  • 6. [Thalassemia-hemoglobin E disease and hypersplenism].
    AKSOY M, CETINGIL AI, KOCABALKAN N, SESTAKOF D, ALADAG T, SECER F, BOSTANCI N.
    Turk Tip Cemiy Mecm; 1962 Apr 28; 28():193-200. PubMed ID: 13859974
    [No Abstract] [Full Text] [Related]

  • 7. The thalassaemia syndromes. I. Thalassaemia minor with large amount of fetal haemoglobin. Study of a family.
    AKSOY M, EGRIBOZLU A, ALPUSTUN H.
    Acta Haematol; 1961 Feb 28; 25():136-42. PubMed ID: 13681961
    [No Abstract] [Full Text] [Related]

  • 8. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 28; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 9. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia.
    Kan YW.
    Schweiz Med Wochenschr Suppl; 1991 Jan 28; 43():51-4. PubMed ID: 1726857
    [Abstract] [Full Text] [Related]

  • 10. Observations on the high foetal haemoglobin gene and its interaction with the thalassaemia gene.
    BARKHAN P, ADINOLFI M.
    J Clin Pathol; 1962 Jul 28; 15(4):350-6. PubMed ID: 13865031
    [Abstract] [Full Text] [Related]

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  • 15. [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
    [No Abstract] [Full Text] [Related]

  • 16. [The recognition of erythrocytes with fetal hemoglobin in peripheral blood smears: possibilities and limitations in the study of thalassemic disease].
    BALLERINI G, CANTELLIT, BELLODI L.
    Haematologica; 1961 Mar 15; 46():443-64. PubMed ID: 13864437
    [No Abstract] [Full Text] [Related]

  • 17. Two families showing interaction of haemoglobin C or thalassaemia with high foetal haemoglobin in adults.
    KRAUS AP, KOCH B, BURCKETT L.
    Br Med J; 1961 May 20; 1(5237):1434-6. PubMed ID: 13754061
    [No Abstract] [Full Text] [Related]

  • 18. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia.
    Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK.
    Am J Hematol; 2013 Jun 20; 88(6):531-2. PubMed ID: 23483609
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  • 20. 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]

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