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    Molecular characterization of HbH disease in the Cuban population

    Molecular characterization of the α-thalassemia mutations present in nine HbH subjects from Cuba was achieved by digestion with Bam HI, Bgl II, and Apa I and hybridization with α- and ζ-specific probes. The re...

    Gisela Martinez, R. Ferreira, Ana Hernandez, Anna Di Rienzo, L. Felicetti in Human Genetics (1986)