Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)
2. The detection of large deletions or duplications in genomic DNA
3. Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes
4. Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene
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