DNA of 15 patients with Duchenne muscular dystrophy (DMD) were analyze
d for deletions within the DMD gene by using recombinant DNA technolog
y. Deletion frequency was 47 percent and six of the deletions occurred
in the region of probe 7 + 8. Only one of the deletions was observed
in the region of probe 9-7, and no deletions were found in the regions
of probe 30-1, 30-2 and 47-4 (5b + 6). The frequency of deletions fou
nd in the Turkish DMD patients corresponds to frequencies reported for
other populations.