Bardet-Biedl and Alström syndromes in Spain

Por Valverde, D, Piñeiro-Gallego, T, Pereiro, I
Publicado em 2012

Molecular approach in the study of Alström syndrome: Analysis of ten Spanish families

Por Piñeiro-Gallego, Teresa, Cortón, Marta, Ayuso, Carmen, Baiget, Montserrat, Valverde, Diana
Publicado em 2012

Clinical evaluation of two consanguineous families with homozygous mutations in BEST1

Por Piñeiro-Gallego, Teresa, Álvarez, María, Pereiro, Inés, Campos, Severiano, Sharon, Dror, Schatz, Patrik, Valverde, Diana
Publicado em 2011

New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: Detection of candidate regions by homozygosity mapping

Por Pereiro, Ines, Valverde, Diana, Piñeiro-Gallego, Teresa, Baiget, Montserrat, Borrego, Salud, Ayuso, Carmen, Searby, Charles, Nishimura, Darryl
Publicado em 2010

Arrayed primer extension technology simplifies mutation detection in Bardet–Biedl and Alström syndrome

Por Pereiro, Ines, Hoskins, Bethan E, Marshall, Jan D, Collin, Gayle B, Naggert, Jürgen K, Piñeiro-Gallego, Teresa, Oitmaa, Eneli, Katsanis, Nicholas, Valverde, Diana, Beales, Philip L
Publicado em 2011