Parcourir Publicaciones UAX par auteur "Villamar, Manuela"

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A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment Gandía, Marta; del Castillo, Francisco J.; Rodríguez Álvarez, Francisco J.; Garrido, Gema; Villamar, Manuela; Calderón, Manuela; Moreno Pelayo, Miguel Angel; Moreno, Felipe; del Castillo, Ignacio Date: 2013-09
Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants Morín, Matias; Borreguero, Lucía; Booth, Kevin T; Lachgar, María; Huygen, Patrick; Villamar, Manuela; Mayo, Fernando; Barrio, Luis Carlos; Santos Serrão de Castro, Luciana; Morales, Carmelo; del Castillo, Ignacio; Arellano, Beatriz; Tellería, Dolores; Smith, Richard J.H.; Azaiez, Hela; Moreno Pelayo, Miguel Angel Date: 2020
Parental Mosaicism in PAX6 Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and Microphthalmia Tarilonte, María; Morín, Matías; Ramos, Patricia; Galdós, Marta; Blanco Kelly, Fiona; Villaverde, Cristina; Rey Zamora, Dolores; Rebolleda, Gema; Muñoz Negrete, Francisco J.; Tahsin Swafiri, Saoud; Gener, Blanca; Moreno Pelayo, Miguel Angel; Ayuso, Carmen; Villamar, Manuela; Corton, Marta Date: 2018-10

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