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Acta Otorrinolaringologica Espanola|July 16, 2004
[Evaluation of a family with sensorineural hearing loss due to the Q829X mutation in the OTOF gene]J Gallo-Terán, R Megía López, C Morales-Angulo, et al.Journal of the American Association for Laboratory Animal Science : JAALAS|July 31, 2015
Assessment of an Orofacial Operant Pain Assay as a Preclinical Tool for Evaluating Analgesic Efficacy in RodentsHarvey E Ramirez, Timothy J Queeney, Misha L Dunbar, et al.Clinical Genetics|November 22, 2007
Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing lossV Labay, G Garrido, A C Madeo, et al.Acta Otorrinolaringologica Espanola|October 14, 2006
[Auditory neuropathy due to the Q829X mutation in the gene encoding otoferlin (OTOF) in an infant screened for newborn hearing impairment]J Gallo-Terán, C Morales-Angulo, N Sánchez, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate geneJ P Hardelin, J Levilliers, I del Castillo, et al.Acta Otorrinolaringologica Espanola|October 6, 2004
[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity]J Gallo-Terán, B Arellano, C Morales-Angulo, et al.Environmental Science and Pollution Research International|November 28, 2013
Prospecting metal-resistant plant-growth promoting rhizobacteria for rhizoremediation of metal contaminated estuaries using Spartina densifloraL Andrades-Moreno, I Del Castillo, R Parra, et al.Cureus|September 12, 2025
Belonging in Hospital Medicine: Insights From Mapping Hospitalists' Priorities for Inclusive Workplace StrategiesHirotaka Kato, Maria I Del Castillo De Calvo, Waliah Muhammad, et al.European Journal of Human Genetics : EJHG|January 1, 1995
Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA familiesE Velasco, C Valero, E García, et al.Human Molecular Genetics|September 1, 1996
A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22I del Castillo, M Villamar, M Sarduy, et al.Pageof 4