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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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Detalles Bibliográficos
Autores principales: 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: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3027091/
https://www.ncbi.nlm.nih.gov/pubmed/21235737
http://dx.doi.org/10.1186/1750-1172-6-2