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Journal Abstract Search

157 related items for PubMed ID: 14942706

  • 1. The population genetics of two inherited blood dyscrasias in man.
    NEEL JV.
    Cold Spring Harb Symp Quant Biol; 1950; 15():141-58. PubMed ID: 14942706
    [No Abstract] [Full Text] [Related]

  • 2. The genetics of human haemoglobin differences: problems and perspectives.
    NEEL JV.
    Ann Hum Genet; 1956 Jul; 21(1):1-30. PubMed ID: 13340556
    [No Abstract] [Full Text] [Related]

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

  • 4. Thalassemia (microkarterocytosis) and drepanocytosis their forms and genetics.
    GATTO I.
    Acta Genet Med Gemellol (Roma); 1953 Jan; 2(1):19-30. PubMed ID: 13016185
    [No Abstract] [Full Text] [Related]

  • 5. Viscosity of sickle cells: a 34-year study of an Italian family with sickle cell and thalassemia traits: splenectomy in two members.
    HAM TH, BATTLE JD.
    Trans Am Clin Climatol Assoc; 1953 Jan; 68():146-53; discussion 153-4. PubMed ID: 13486615
    [No Abstract] [Full Text] [Related]

  • 6. A family illustrating the double inheritance of the sickle cell trait and of Mediterranean anaemia.
    HUMBLE JG, ANDERSON I, WHITE JC, FREEMAN T.
    J Clin Pathol; 1954 Aug; 7(3):201-8. PubMed ID: 13192194
    [No Abstract] [Full Text] [Related]

  • 7. Abnormal forms of hemoglobin from a genetic point of view.
    NEEL JV.
    AMA Arch Intern Med; 1956 Nov; 98(5):555-8. PubMed ID: 13361589
    [No Abstract] [Full Text] [Related]

  • 8. 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; 12(7):593-602. PubMed ID: 13436515
    [No Abstract] [Full Text] [Related]

  • 9. [Contribution to the knowledge of Silvestroni-Bianco disease].
    VENTRUTO V, DINI E, QUATTRIN N.
    Haematologica; 1961 Jul; 46():965-84. PubMed ID: 13925345
    [No Abstract] [Full Text] [Related]

  • 10. [Observations on the distribution of Mediterranean and drepanocytic anomalies in 3 Calabrese families].
    GIGANTE D, SANTAGATI U, GHIONE R.
    Acta Genet Med Gemellol (Roma); 1960 Apr; 9():211-33. PubMed ID: 13849952
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. The human hemoglobins in health and disease.
    CHERNOFF AI.
    N Engl J Med; 1955 Sep 08; 253(10):416-23; concl. PubMed ID: 13253850
    [No Abstract] [Full Text] [Related]

  • 13. Sickle-cell thalassaemia disease in a family with intermarriage of siblings.
    BUDTZ-OLSEN OE, BELL K, HILLCOAT BL, NEWCOMBE RL.
    Med J Aust; 1961 Dec 02; 48(2)():902-4. PubMed ID: 13874388
    [No Abstract] [Full Text] [Related]

  • 14. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 02; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 15. Are certain blood dyscrasias an effect of racial mixture?
    ASHMAN R.
    Am J Phys Anthropol; 1952 Jun 02; 10(2):217-23. PubMed ID: 14952570
    [No Abstract] [Full Text] [Related]

  • 16. [Thalassemia minima].
    GATTO I, VALENTINO L.
    Boll Soc Ital Biol Sper; 1952 May 02; 28(5):1049-50. PubMed ID: 13018618
    [No Abstract] [Full Text] [Related]

  • 17. Thalassemia in Jews from Kurdistan.
    MATOTH Y, SHAMIR Z, FREUNDLICH E.
    Blood; 1955 Feb 02; 10(2):176-89. PubMed ID: 13230170
    [No Abstract] [Full Text] [Related]

  • 18. [Thalassemia and neurohemolytic syndromes].
    SARROUY C, CABANNES R, SENDRA L, ZEVACO P.
    Bull Mem Soc Med Hop Paris; 1955 Feb 02; 68(22-23):825-30. PubMed ID: 12978864
    [No Abstract] [Full Text] [Related]

  • 19. Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin.
    NEEL JV, ITANO HA, LAWRENCE JS.
    Blood; 1953 May 02; 8(5):434-43. PubMed ID: 13041746
    [No Abstract] [Full Text] [Related]

  • 20. Thalassaemia in a Scottish family.
    ISRAELS LG, SUDERMAN HJ, HOOGSTRATEN J.
    Lancet; 1955 Dec 24; 269(6904):1318-20. PubMed ID: 13272382
    [No Abstract] [Full Text] [Related]

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