Bardet-Biedl and Alström syndromes in Spain

por Valverde, D, Piñeiro-Gallego, T, Pereiro, I
Publicado 2012

Performing whole-exome sequencing in Bardet-Bield syndrome

por Castro-Sánchez, S, Alvarez-Satta, M, Valverde, D
Publicado 2015

Human regulatory proteins associate with non-coding RNAs from the EBV IR1 region

por Tompkins, V. S., Valverde, D. P., Moss, W. N.
Publicado 2018

DNA Methylation and Ciliopathies: a way to be explored

por Alvarez-Satta, M, Chiara, L De, Castro-Sánchez, S, Valverde, D
Publicado 2015

Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease

por Riveiro-Alvarez, R., Valverde, D., Lorda-Sanchez, I., Trujillo-Tiebas, M. J., Cantalapiedra, D., Vallespin, E., Aguirre-Lamban, J., Ramos, C., Ayuso, C.
Publicado 2007