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Right here, we applied in-depth hereditary analyses to a series of 29 osteoblastomas, including five classified as epithelioid osteoblastoma. We found recurrent homozygous deletions for the NF2 gene in three associated with five epithelioid instances and in one main-stream osteoblastoma. These events had been mutually exclusive from FOS mutations. Structural variations were based on deep whole gen
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