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- 2020
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Mark
Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma
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- Contribution to journal › Article
- 2014
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Mark
GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.
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- Contribution to journal › Article
- 2013
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Mark
Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the wnt/beta-catenin signaling pathway.
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- Contribution to journal › Article
- 2012
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Mark
Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches
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- Contribution to journal › Article
- 2011
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Mark
Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study
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- Contribution to journal › Article
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Mark
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
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- Contribution to journal › Article
- 2010
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Mark
Heterogeneous and Complex Rearrangements of Chromosome Arm 6q in Chondromyxoid Fibroma. Delineation of Breakpoints and Analysis of Candidate Target Genes.
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- Contribution to journal › Article
- 2009
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Mark
No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies
(
- Contribution to journal › Article