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1 exposure or any other clinical features (non-syndromic hearing loss).
2 e the major cause of autosomal recessive non-syndromic hearing loss.
3 multiple mitochondrial dysfunctions, and non-syndromic hearing loss.
4 sociated with aminoglycoside-induced and non-syndromic hearing loss.
5 iously shown to cause both syndromic and non-syndromic hearing loss.
6 role in the phenotypic manifestation of non-syndromic hearing loss and aminoglycoside toxicity assoc
7 ing dermatological disorders associated with syndromic hearing loss and cover a wide range of severit
8 individuals from the midwestern USA with non-syndromic hearing loss and dilated vestibular aqueducts
9 f inner-ear architecture associated with non-syndromic hearing loss, and suggest that tectorial membr
10 ecessive forms of nonsyndromic hearing loss, syndromic hearing loss, and, in some cases, even multipl
11 e DFNB7/11 locus for autosomal recessive non-syndromic hearing loss (ARNSHL) has been mapped to an ap
12 this gene also cause autosomal dominant non-syndromic hearing loss as a dominant-negative consequenc
13 Pendred syndrome and autosomal recessive non-syndromic hearing loss at the DFNB4 locus on chromosome
14 hancers in which mutations could lead to non-syndromic hearing loss, craniofacial defects or limb mal
16 s lead to early-onset autosomal dominant non-syndromic hearing loss, familial thoracic aortic aneurys
23 The genetics of both syndromic (SHL) and non-syndromic hearing loss (NSHL) is characterized by a high
24 and one Dutch) with autosomal dominant, non-syndromic hearing loss to have mutations in COL11A2 that
25 ations reported only in individuals with non-syndromic hearing loss (V480D, V653A and I490L/G497S).
27 y from PDS mutations in individuals with non-syndromic hearing loss, we compared three common Pendred
28 ation in which hypomorphic alleles cause non-syndromic hearing loss, while more severe mutations of t
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