Sommaire

Publications 2011

Nos publications

Documents

A novel DCC mutation and genetic heterogeneity in congenital mirror movements

Lire

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

Lire

Diagnostic and prognostic value of alpha internexin expression in a series of 409 gliomas

Lire

Methylation profiling identifies 2 groups of gliomas according to their tumorigenesis

Lire

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

Lire

REEP1 Mutations in SPG31: Frequency, Mutational Spectrum, and Potential Association with Mitochondrial Morpho-Functional Dysfunction

Lire

Sur le même sujet