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Further delineation of the DFNA5 phenotype: results of speech recognition tests.
De Leenheer EM, van Zuijlen DA, Van Laer L, Van Camp G, Huygen PL, Huizing EH, Cremers CW. De Leenheer EM, et al. Among authors: van laer l, van zuijlen da, van camp g. Ann Otol Rhinol Laryngol. 2002 Jul;111(7 Pt 1):639-41. doi: 10.1177/000348940211100712. Ann Otol Rhinol Laryngol. 2002. PMID: 12126021
DFNA5, a gene involved in hearing loss and cancer: a review.
de Beeck KO, Van Laer L, Van Camp G. de Beeck KO, et al. Among authors: van laer l, van camp g. Ann Otol Rhinol Laryngol. 2012 Mar;121(3):197-207. doi: 10.1177/000348941212100310. Ann Otol Rhinol Laryngol. 2012. PMID: 22530481 Review.
Clinical features of DFNA5.
De Leenheer EM, van Zuijlen DA, Van Laer L, Van Camp G, Huygen PL, Huizing EH, Cremers CW. De Leenheer EM, et al. Among authors: van laer l, van zuijlen da, van camp g. Adv Otorhinolaryngol. 2002;61:53-9. doi: 10.1159/000066800. Adv Otorhinolaryngol. 2002. PMID: 12408063 No abstract available.
Nonsyndromic hearing impairment is associated with a mutation in DFNA5.
Van Laer L, Huizing EH, Verstreken M, van Zuijlen D, Wauters JG, Bossuyt PJ, Van de Heyning P, McGuirt WT, Smith RJ, Willems PJ, Legan PK, Richardson GP, Van Camp G. Van Laer L, et al. Among authors: van de heyning p, van zuijlen d, van camp g. Nat Genet. 1998 Oct;20(2):194-7. doi: 10.1038/2503. Nat Genet. 1998. PMID: 9771715
DFNA10/EYA4--the clinical picture.
De Leenheer EM, Huygen PL, Wayne S, Verstreken M, Declau F, Van Camp G, Van de Heyning PH, Smith RJ, Cremers CW. De Leenheer EM, et al. Among authors: van de heyning ph, van camp g. Adv Otorhinolaryngol. 2002;61:73-8. doi: 10.1159/000066807. Adv Otorhinolaryngol. 2002. PMID: 12408066 No abstract available.
553 results