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	1.	Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p. [electronic resource] by Gurrieri, Fiorella Zollino, Marcella Oliva, Antonio Pascali, Vincenzo Orteschi, Daniela Pietrobono, Roberta Camporeale, Antonella Coll Vidal, Monica Partemi, Sara Brugada, Ramon Bellocci, Fulvio Neri, Giovanni Producer: 20140324 In: European journal of human genetics : EJHG vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation. [electronic resource] by Parisi, Pasquale Oliva, Antonio Coll Vidal, Monica Partemi, Sara Campuzano, Oscar Iglesias, Anna Pisani, Daniela Pascali, Vincenzo L Paolino, Maria Chiara Villa, Maria Pia Zara, Federico Tassinari, Carlo Alberto Striano, Pasquale Brugada, Ramon Producer: 20140214 In: Epilepsy research vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Genetic analysis, in silico prediction, and family segregation in long QT syndrome. [electronic resource] by Riuró, Helena Campuzano, Oscar Berne, Paola Arbelo, Elena Iglesias, Anna Pérez-Serra, Alexandra Coll-Vidal, Mònica Partemi, Sara Mademont-Soler, Irene Picó, Ferran Allegue, Catarina Oliva, Antonio Gerstenfeld, Edward Sarquella-Brugada, Georgia Castro-Urda, Víctor Fernández-Lozano, Ignacio Mont, Lluís Brugada, Josep Scornik, Fabiana S Brugada, Ramon Producer: 20150805 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)