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PUBMED FOR HANDHELDS

Journal Abstract Search


234 related items for PubMed ID: 13436515

  • 21. [Apropos of a study of hemoglobin in anemic patients].
    FARHAT M, BOUJNAH A.
    Tunis Med; 1962; 40():431-43. PubMed ID: 13944362
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  • 25. [Thalassemia, hemoglobin H disease and persistent Bart's hemoglobin in a Jewish family from Iraq].
    RAMOTH B, SHEBA C, FISHER S.
    Harefuah; 1960 Jan 01; 58():1-3. PubMed ID: 14436103
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  • 29. [High hemoglobin A-2 disease and microcythemia].
    LUCCI R, SOFFRITTI E, BORGATTI L, CABASSA N.
    Acta Genet Med Gemellol (Roma); 1962 Jan 01; 11():71-88. PubMed ID: 14467126
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  • 31. HEREDITARY RED CELL TRAITS AND MALARIA.
    MOTULSKY AG.
    Am J Trop Med Hyg; 1964 Jan 01; 13():SUPPL147-58. PubMed ID: 14106725
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  • 32. Hemoglobin-S-thalassemia disease; report of a case in a Negro child.
    SHIELDS GS, WETHERS D, GAVIS G, WATSON RJ.
    AMA J Dis Child; 1956 May 01; 91(5):485-9. PubMed ID: 13312885
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  • 33. 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
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  • 34. 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
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  • 35. Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.
    Felice AE, Ozdonmez R, Headlee ME, Huisman TH.
    Biochem Genet; 1982 Aug 02; 20(7-8):689-701. PubMed ID: 6291506
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  • 37. [First case of hemoglobin C-thalassemia in Italy].
    PEROSA L, MANGANELLI G, DALFINO G.
    Boll Soc Ital Biol Sper; 1960 Feb 15; 36():93-6. PubMed ID: 14431935
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  • 38. RELATIONSHIP OF HEMOGLOBIN BART'S AND H TO ALPHA THALASSEMIA.
    WEATHERALL DJ.
    Ann N Y Acad Sci; 1964 Oct 07; 119():463-73. PubMed ID: 14219426
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