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Audiologic and genetic characterization of hearing loss in Osteogenesis Imperfecta
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The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss
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Longitudinal and cross-sectional phenotype analysis in a new, large dutch DFNA2/KCNQ4 family.
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Further delineation of the DFNA5 phenotype: Results of speech recognition tests
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A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.
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The DFNA10 phenotype.
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tHE PRESENCE OF A WIDENED VESTIBULAR AQUADUCT AND PROGRESSIVE SENSORINEURAL HEARING LOSS IN THE BRANCHIO OTO RENAL SYNROME
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Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH.