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EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

Osteochondromas occur as sporadic solitary lesions or as multiple lesions, characterizing the hereditary multiple exostoses syndrome (EXT). Approximately 15% of all chondrosarcomas arise within the cartilaginous cap of an osteochondroma. EXT is genetically heterogeneous, and two genes, EXT1 and EXT2...

詳細記述

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書誌詳細
主要な著者: Bovée, J V, Cleton-Jansen, A M, Wuyts, W, Caethoven, G, Taminiau, A H, Bakker, E, Van Hul, W, Cornelisse, C J, Hogendoorn, P C
フォーマット: Artigo
言語:Inglês
出版事項: 1999
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377975/
https://ncbi.nlm.nih.gov/pubmed/10441575
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