Publications

CIC inactivating mutations identify aggressive subset of 1p19q codeleted gliomas

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A novel DCC mutation and genetic heterogeneity in congenital mirror movements

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Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females

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Chromosome 7p11.2 (EGFR) variation influences glioma risk

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RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans

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