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Journal Abstract Search

259 related items for PubMed ID: 2454217

  • 1. Genetic heterogeneity of thalassemias in Mexican mestizo patients with hemolytic anemia.
    Ibarra B, Vaca G, de la Mora E, Romero F, Aguilar-Luna C, Mejía A, Esparza MA, Pérez G, Ornelas ML, Cantú JM.
    Hum Hered; 1988; 38(2):95-100. PubMed ID: 2454217
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  • 2. [Abnormal hemoglobins and thalassemias in Mexico].
    Ruiz-Reyes G.
    Rev Invest Clin; 1998; 50(2):163-70. PubMed ID: 9658939
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  • 8. A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.
    Di Iorio EE, Winterhalter KH, Wilson K, Rosenmund A, Marti HR.
    Blut; 1975 Aug; 31(2):61-8. PubMed ID: 1164567
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  • 9. DNA-polymorphic patterns linked to the beta-globin genes in German families affected with hemoglobinopathies and thalassemias: a comparison to other ethnic groups.
    Oehme R, Kohne E, Horst J.
    Hum Genet; 1985 Aug; 71(3):219-22. PubMed ID: 2998970
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  • 10. [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 Aug; 46(1):22-33. PubMed ID: 4731929
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  • 12. Hematological and molecular analysis of beta-thalassemia and Hb Lepore in Campania, Italy.
    Ferrara M, Matarese SM, Francese M, Borrelli B, Coppola L, Coppola A, Esposito L.
    Hemoglobin; 2001 Feb; 25(1):29-34. PubMed ID: 11300347
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  • 16. [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 Feb; 18(2):145-56. PubMed ID: 4753554
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