Genome-wide analysis of Ollier disease: Is it all in the genes?

BACKGROUND: Ollier disease is a rare, non-hereditary disorder which is characterized by the presence of multiple enchondromas (ECs), benign cartilaginous neoplasms arising within the medulla of the bone, with an asymmetric distribution. The risk of malignant transformation towards central chondrosar...

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Detalhes bibliográficos
Main Authors: Pansuriya, Twinkal C, Oosting, Jan, Krenács, Tibor, Taminiau, Antonie HM, Verdegaal, Suzan HM, Sangiorgi, Luca, Sciot, Raf, Hogendoorn, Pancras CW, Szuhai, Karoly, Bovée, Judith VMG
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3027091/
https://ncbi.nlm.nih.gov/pubmed/21235737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-2
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