Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell haemangioma in Ollier disease and Maffucci syndrome
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ABSTRACT: This SuperSeries is composed of the following subset Series: GSE30354: Examination of Ollier Disease and Maffucci Syndrome using IDH Tiling Array GSE30835: mRNA expression data of tumor samples with/without IDH1/2 mutations GSE31337: Methylation profiling of enchondromas with and without IDH1 mutations Refer to individual Series
ORGANISM(S): Homo sapiens
SUBMITTER: Twinkal Pansuriya
PROVIDER: E-GEOD-30844 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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