Browsing by Author "Monnier, N."
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- ItemThe neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis(2013) Dieterich, K.; Quijano-Roy, S.; Monnier, N.; Zhou, J.; Fauré, J.; Smirnow, D.A.; Carlier, R.; Laroche, C.; Marcorelles, P.; Mercier, S.; Mégarbané, A.; Odent, S.; Romero, N.; Sternberg, D.; Marty, I.; Estournet, B.; Jouk, P.; Melki, J.; Lunardi, J.
- ItemWhole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutations(2012) Jarraya, M.; Quijano-Roy, S.; Monnier, N.; Béhin, A.; Avila-Smirnov, D.; Romero, N.B.; Allamand, V.; Richard, P.; Barois, A.; May, A.; Estournet, B.; Mercuri, E.; Carlier, P.G.; Carlier, R.-Y.