| 摘要 |
<p>The present invention provides methods for detecting and mapping chromosomal rearrangements associated with various diseases using comparative genomic hybridization. Included are methods to identify translocation partners of known genomic loci and to determine translocation breakpoints. The methods of the present invention may also be used in the prognosis, diagnosis, and determination of predisposition to diseases that involve chromosomal rearrangements such as translocations.</p> |
