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Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell haemangioma in Ollier disease and Maffucci syndrome
PubMed Full text in PMC Similar studies Analyze with GEO2R
Illumina HumanWG-6 v3.0 expression beadchip
Agilent-032447 Custom Human IDH Array
Illumina HumanMethylation27 BeadChip (HumanMethylation27_270596_v.1.2)
MAF250
L2463
L2357
L2103a
L2100
L1829
L1686
L1598
L1251
L198
L194
L1684
L2386
L2280
L2218
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