Genetic and electrophoretic studies in three Greek families inheriting the traits for both sickling and thalassemia


Seven patients with hemoglobin S-thalassemia disease belonging to three Greek families are described. Interaction of the genes for hemoglobin S and for thalassemia was evident in all but one cases. Hemoglobin analyses consisting of a combination of paper electrophoresis and the alkali denaturation technic revealed the S+A+F pattern in three, the S+F+A… (More)
DOI: 10.1007/BF01633483

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