A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22....

por Quintela, Ines, Fernandez-Prieto, Montse, Gomez-Guerrero, Lorena, Resches, Mariela, Eiris, Jesus, Barros, Francisco, Carracedo, Angel
Publicado 2015

Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders

por Fernández-Marmiesse, Ana, Morey, Marcos, Pineda, Merce, Eiris, Jesús, Couce, Maria Luz, Castro-Gago, Manuel, Fraga, Jose Maria, Lacerda, Lucia, Gouveia, Sofia, Pérez-Poyato, Maria Socorro, Armstrong, Judith, Castiñeiras, Daisy, Cocho, Jose A
Publicado 2014

Evolutionary Analyses of Entire Genomes Do Not Support the Association of mtDNA Mutations with Ras/MAPK Pathway Syndromes

por Gómez-Carballa, Alberto, Cerezo, María, Balboa, Emilia, Heredia, Claudia, Castro-Feijóo, Lidia, Rica, Itxaso, Barreiro, Jesús, Eirís, Jesús, Cabanas, Paloma, Martínez-Soto, Isabel, Fernández-Toral, Joaquín, Castro-Gago, Manuel, Pombo, Manuel, Carracedo, Ángel, Barros, Francisco, Salas, Antonio
Publicado 2011

Health care and societal costs of the management of children and adolescents with attention-deficit/hyperactivity disorder in Spain: a descriptive analysis

por Quintero, Javier, Ramos-Quiroga, Josep A., Sebastián, Javier San, Montañés, Francisco, Fernández-Jaén, Alberto, Martínez-Raga, José, Giral, Marta García, Graell, Montserrat, Mardomingo, María J., Soutullo, César, Eiris, Jesús, Téllez, Montserrat, Pamias, Montserrat, Correas, Javier, Sabaté, Juncal, García-Orti, Laura, Alda, José A.
Publicado 2018