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Acta Otorrinolaringologica Espanola|October 26, 2005
[Molecular genetic study of Usher syndrome in Spain]T Jaijo, E Aller, M Beneyto, et al.Archivos De La Sociedad Espanola De Oftalmologia|December 17, 2008
[Genetic counselling in visual and auditory disorders]J M Millán, E Aller, T Jaijo, et al.Clinical Genetics|November 4, 2004
Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variabilityE Aller, T Jaijo, S Oltra, et al.Human Mutation|April 23, 2008
Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type IA Oshima, T Jaijo, E Aller, et al.Clinical Genetics|September 18, 2012
Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depthT Sevilla, D Martínez-Rubio, C Márquez, et al.Neuromuscular Disorders : NMD|September 17, 2016
Phenotypic heterogeneity in two large Roma families with a congenital myasthenic syndrome due to CHRNE 1267delG mutation. A long-term follow-upD Natera-de Benito, J Domínguez-Carral, N Muelas, et al.Clinical Genetics|May 26, 2010
Functional analysis of splicing mutations in MYO7A and USH2A genesT Jaijo, E Aller, M J Aparisi, et al.Human Mutation|February 14, 2006
Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type IT Jaijo, E Aller, S Oltra, et al.Journal of Medical Genetics|November 7, 2006
Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type IIE Aller, T Jaijo, M Beneyto, et al.Pageof 1