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	1.	Spinocerebellar Ataxia 27: Clinical Phenotype of Twin Sisters with FGF14 Deletion. [electronic resource] by Amado, Alfonso Blanco, Manuel Oscar Repáraz-Andrade, Alfredo Producer: 20180524 In: Neuropediatrics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Neurodevelopmental Disorders and Array-Based Comparative Genomic Hybridization: Sensitivity and Specificity using a Criteria Checklist for Genetic Test Performance. [electronic resource] by Amado-Puentes, Alfonso Reparaz-Andrade, Alfredo Del Campo-García, Aida Blanco-Barca, Manuel Óscar Salgado-Barreira, Ángel Del Campo-Pérez, Víctor Fernández-Lorenzo, José Ramón Producer: 20191230 In: Neuropediatrics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability. [electronic resource] by Gimeno-Ferrer, Fátima Albuquerque, David Guzmán Luján, Carola Marcaida Benito, Goitzane Torreira Banzas, Cristina Repáraz-Andrade, Alfredo Ballesteros Cogollos, Virginia Aleu Pérez-Gramunt, Montserrat Galán Gómez, Enrique Quintela, Inés Rodríguez-López, Raquel Producer: 20190410 In: Journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients. [electronic resource] by Cabanillas, Rubén Diñeiro, Marta Cifuentes, Guadalupe A Castillo, David Pruneda, Patricia C Álvarez, Rebeca Sánchez-Durán, Noelia Capín, Raquel Plasencia, Ana Viejo-Díaz, Mónica García-González, Noelia Hernando, Inés Llorente, José L Repáraz-Andrade, Alfredo Torreira-Banzas, Cristina Rosell, Jordi Govea, Nancy Gómez-Martínez, Justo Ramón Núñez-Batalla, Faustino Garrote, José A Mazón-Gutiérrez, Ángel Costales, María Isidoro-García, María García-Berrocal, Belén Ordóñez, Gonzalo R Cadiñanos, Juan Producer: 20190731 In: BMC medical genomics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy. [electronic resource] by Ochoa, Juan Pablo Sabater-Molina, María García-Pinilla, José Manuel Mogensen, Jens Restrepo-Córdoba, Alejandra Palomino-Doza, Julián Villacorta, Eduardo Martinez-Moreno, Marina Ramos-Maqueda, Javier Zorio, Esther Peña-Peña, Maria L García-Granja, Pablo E Rodríguez-Palomares, José F Cárdenas-Reyes, Ivonne J de la Torre-Carpente, María M Bautista-Pavés, Alicia Akhtar, Mohammed M Cicerchia, Marcos N Bilbao-Quesada, Raquel Mogollón-Jimenez, Maria Victoria Salazar-Mendiguchía, Joel Mesa Latorre, José M Arnaez, Blanca Olavarri-Miguel, Ivan Fuentes-Cañamero, María E Lamounier, Arsonval Pérez Ruiz, José María Climent-Payá, Vicente Pérez-Sanchez, Inmaculada Trujillo-Quintero, Juan P Lopes, Luis R Repáraz-Andrade, Alfredo Marín-Iglesias, Rosario Rodriguez-Vilela, Alejandro Sandín-Fuentes, María Garrote, Jose A Cortel-Fuster, Alejandro Lopez-Garrido, Miguel Fontalba-Romero, Ana Ripoll-Vera, Tomás Llano-Rivas, Isabel Fernandez-Fernandez, Xusto Isidoro-García, María Garcia-Giustiniani, Diego Barriales-Villa, Roberto Ortiz-Genga, Martín García-Pavía, Pablo Elliott, Perry M Gimeno, Juan R Monserrat, Lorenzo Producer: 20190912 In: Journal of the American College of Cardiology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)