Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach

por Córdoba, Marta, Rodriguez-Quiroga, Sergio Alejandro, Vega, Patricia Analía, Salinas, Valeria, Perez-Maturo, Josefina, Amartino, Hernán, Vásquez-Dusefante, Cecilia, Medina, Nancy, González-Morón, Dolores, Kauffman, Marcelo Andrés
Publicado 2018

Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders

por González-Morón, Dolores, Vishnopolska, Sebastián, Consalvo, Damián, Medina, Nancy, Marti, Marcelo, Córdoba, Marta, Vazquez-Dusefante, Cecilia, Claverie, Santiago, Rodríguez-Quiroga, Sergio Alejandro, Vega, Patricia, Silva, Walter, Kochen, Silvia, Kauffman, Marcelo Andrés
Publicado 2017

Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder

por Nemirovsky, Sergio I., Córdoba, Marta, Zaiat, Jonathan J., Completa, Sabrina P., Vega, Patricia A., González-Morón, Dolores, Medina, Nancy M., Fabbro, Mónica, Romero, Soledad, Brun, Bianca, Revale, Santiago, Ogara, María Florencia, Pecci, Adali, Marti, Marcelo, Vazquez, Martin, Turjanski, Adrián, Kauffman, Marcelo A.
Publicado 2015