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| Issue Date | Title | Author(s) |
|---|---|---|
| 14-Jul-2017 | Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder | García Martínez, Iris; Sánchez Mora, Cristina; Soler Artigas, María; Rovira, Paula; Pagerols Teixidó, Mireia; Corrales, Montserrat; Calvo Sánchez, Eva; Richarte, Vanesa; Bustamante Pineda, Mariona; Sunyer Deu, Jordi; Cormand Rifà, Bru; Casas, Miquel; Ramos Quiroga, Josep Antoni; Ribasés Haro, Marta |
| 31-Aug-2017 | Association of the PLCB1 gene with drug dependence | Cabana Domínguez, Judit; Roncero, Carlos; Pineda Cirera, Laura; Palma Álvarez, R. Felipe; Ros Cucurull, Elena; Grau-López, Lara; Esojo, Abderaman; Casas, Miquel; Arenas Solà, Concepción; Ramos Quiroga, Josep Antoni; Ribasés Haro, Marta; Fernàndez Castillo, Noèlia; Cormand Rifà, Bru |
| 31-May-2017 | Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia | Sintas Vives, Cèlia; Carreño, Oriel; Fernàndez Castillo, Noèlia; Corominas Castiñeira, Roser; Vila Pueyo, Marta; Toma, Claudio; Cuenca León, Ester; Barroeta, Isabel; Roig i Arnall, Carles; Volpini Bertrán, Víctor; Macaya Ruiz, Alfons; Cormand Rifà, Bru |
| 10-Mar-2017 | A de novo nonsense mutation in MAGEL2 in a patient initially diagnosed as Opitz-C: Similarities between Schaaf-Yang and Opitz-C syndromes | Urreizti, Roser; Cueto Gonzalez, Anna Maria; Franco Valls, Héctor; Mort Farre, Sílvia; Roca Ayats, Neus; Ponomarenko, Julia; Cozzuto, Luca; Company, Carlos; Bosio, Mattia; Ossowski, Stephan; Montfort Roca, Magda; Hecht, Jochen; Tizzano Ferrari, Eduardo; Cormand Rifà, Bru; Vilageliu i Arqués, Lluïsa; Opitz, John M.; Neri, Giovanni; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |