Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders

por Homs, A, Codina-Solà, M, Rodríguez-Santiago, B, Villanueva, C M, Monk, D, Cuscó, I, Pérez-Jurado, L A
Publicado 2016

Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing

por van Eyk, C. L., Webber, D. L., Minoche, A. E., Pérez-Jurado, L. A., Corbett, M. A., Gardner, A. E., Berry, J. G., Harper, K., MacLennan, A. H., Gecz, J.
Publicado 2021