[HTML][HTML] Sensorineural hearing loss due to a novel mutation in the PCDH15 gene: A case study
Sensory deafness is a disorder with a broad spectrum of phenotypes. It is associated with
genetic heterogeneity, thus making sequential single-gene testing an impractical basis for …
genetic heterogeneity, thus making sequential single-gene testing an impractical basis for …
Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: Findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth …
Background The genetic basis of hearing loss in humans is relatively poorly understood. In
recent years, experimental approaches including laboratory studies of early onset hearing …
recent years, experimental approaches including laboratory studies of early onset hearing …
[PDF][PDF] Influência das alterações vestibulares no aprendizado espacial e retenção de memória em camundongos mutantes equilíbrio (Nox3eqlb), mergulhador …
NB Pellagio, SMG Massironi, CMC Mori - 29. SIICUSP: resumos, 2021 - repositorio.usp.br
INFLUÊNCIA DAS ALTERAÇÕES VESTIBULARES NO APRENDIZADO ESPACIAL E RETENÇÃO
DE MEMÓRIA EM CAMUNDONGOS MUTANTES EQUILÍBRIO P Page 1 INFLUÊNCIA DAS …
DE MEMÓRIA EM CAMUNDONGOS MUTANTES EQUILÍBRIO P Page 1 INFLUÊNCIA DAS …
[引用][C] Clinical and Genetic Characterization of Syndromic and Non-syndromic Hearing Impairment in Consanguineous Families
A NASIR