DFNB21
Similar articles
-
Clinical presentation of DFNA8-DFNA12.Adv Otorhinolaryngol. 2002;61:60-5. doi: 10.1159/000066805. Adv Otorhinolaryngol. 2002. PMID: 12408064 No abstract available.
-
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.J Med Genet. 2003 May;40(5):360-3. doi: 10.1136/jmg.40.5.360. J Med Genet. 2003. PMID: 12746400 Free PMC article. No abstract available.
-
Histopathology of nonsyndromic autosomal dominant midfrequency sensorineural hearing loss.Otol Neurotol. 2008 Aug;29(5):601-6. doi: 10.1097/MAO.0b013e3181778245. Otol Neurotol. 2008. PMID: 18665028 Free PMC article.
-
The tectorial membrane: one slice of a complex cochlear sandwich.Curr Opin Otolaryngol Head Neck Surg. 2008 Oct;16(5):458-64. doi: 10.1097/MOO.0b013e32830e20c4. Curr Opin Otolaryngol Head Neck Surg. 2008. PMID: 18797289 Free PMC article. Review.
-
[From gene to disease; DFNA8/12, an autosomal dominant inherited bowl-shaped sensorineural hearing impairment].Ned Tijdschr Geneeskd. 2007 Mar 3;151(9):531-4. Ned Tijdschr Geneeskd. 2007. PMID: 17373394 Review. Dutch.
Cited by
-
Molecular genetics of non-syndromic deafness.Braz J Otorhinolaryngol. 2005 Mar-Apr;71(2):216-23. doi: 10.1016/s1808-8694(15)31313-6. Epub 2005 Aug 2. Braz J Otorhinolaryngol. 2005. PMID: 16446920 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical