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Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families
BACKGROUND: Osteochondromas (cartilage-capped bone tumors) are by far the most commonly treated of all primary benign bone tumors (50%). In 15% of cases, these tumors occur in the context of a hereditary syndrome called multiple osteochondromas (MO), an autosomal dominant skeletal disorder character...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3152881/ https://ncbi.nlm.nih.gov/pubmed/21703028 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-85 |
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