Sfoglia Publicaciones UAX per Autore "Smith, Richard J.H."

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DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Non-syndromic Autosomal Dominant Hearing Loss Hildebrand, Michael S.; Morín, Matías; Meyer, Nicole C.; Mayo, Fernando; Modamio Hoybjor, Silvia; Mencía, Angeles; Olavarrieta, Leticia; Morales Angulo, Carmelo; Nishimura, Carla J.; Workman, Heather; DeLuca, Adam P.; del Castillo, Ignacio; Taylor, Kyle R.; Tompkins, Bruce; Goodman, Corey W.; Schrauwen, Isabelle; Van Wesemael, Maarten; Lachlan, K.; Shearer, A. Eliot; Braun, Terry A.; Huygen, Patrick L.M.; Kremer, Hannie; Van Camp, Guy; Moreno, Felipe; Casavant, Thomas L.; Smith, Richard J.H.; Moreno Pelayo, Miguel Angel Data: 2011-07
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 Data: 2020

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