Beta-thalassemia is a major hereditary blood disorder in Iran. This disease is more prevalent in provinces of the south and north of Iran. In this mutational screening study using ARMS/PCR technique was conducted on 104 blood samples of thalassemic patients from Bushehr Province who receiving regular blood transfusions. We used 12 ARMS primers. Mutations in 81.73% of chromosomes were detected. The frequency of detected mutations were the following: IvI 3' end (24.04%), IvsII-1 (12.98%), IvsI-1 (9.13%), Fr 8,9 (8.17%), IvsI-5 (7.69%), IvsI-110 (5. 77%), codon 30 (3.36%), codun 39 (3.36%), IvsII-745 (3.36%), codon 5 (2.40%), IvsaI-6(1.44%); and no codon 44 mutation was detected. Therefore, the most common mutation among thalassemic patient in Bushehr Province was - 25bp deletion in IvsI.