Luis Pérez-Jurado

Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders.

Rui Bernardes, Miguel Castelo-Branco, Aldina Reis, 2007, The Journal of clinical investigation.

Assessment of copy number variation using the Illumina Infinium 1M SNP‐array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study

Alfonso Valencia, Daniel Rico, Núria Malats, 2011, Human mutation.