Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell haemangioma in Ollier disease and Maffucci syndrome

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