| 摘要 |
<p>The human DMD probe comprising a single-stranded nucleic acid sequence capable of hybridizing to a region of DNA on a human X chromosome between the deletion break point at Xp21.3 and the translocation break point at X;11, the nucleic acid sequence being incapable of hybridizing concurrently to the region of DNA between the deletion break point at Xp21.3 and the terminus of the X chromosome, and to the region of DNA between the translocation point at X;11 and the centromere of the X chromosome.</p> |
