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- Seven polymorphic sites in the beta-globin cluster in association with specific thalassemia mutations were analyzed in a sample from Sardinia (Italy). In order to verify previous works carried out on normal samples (betaA/betaA) and family studies on beta-thalassemia homozygotes individuals, the haplotype frequencies in both normal individuals (betaA/betaA) and betadeg39-thalassemia carriers (beta...
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