Title: Genome-wide analysis of Ollier disease: Is it all in the genes?
Authors: Pansuriya, Twinkal C ×
Oosting, Jan
Krenacs, Tibor
Taminiau, Antonie H. M
Verdegaal, Suzan H. M
Sangiorgi, Luca
Sciot, Raf
Hogendoorn, Pancras C. W
Szuhai, Karoly
Bovee, Judith V. M. G #
Issue Date: Jan-2011
Publisher: BioMed Central
Series Title: Orphanet Journal of Rare Diseases vol:6 issue:1
Article number: 2
Abstract: 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 chondrosarcoma (CS) is increased up to 35%. The aetiology of Ollier disease is unknown.
ISSN: 1750-1172
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Translational Cell & Tissue Research
× corresponding author
# (joint) last author

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