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Quoted phrase not found in phrase index: "Hearing loss, autosomal recessive 112"
Page 1
Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa.
Pieke-Dahl S, Ohlemiller KK, McGee J, Walsh EJ, Kimberling WJ. Pieke-Dahl S, et al. Hear Res. 1997 Oct;112(1-2):1-12. doi: 10.1016/s0378-5955(97)00087-7. Hear Res. 1997. PMID: 9367224
The Usher syndromes (US) are a group of inherited disorders that feature autosomal recessive neurosensory hearing loss or deafness with retinitis pigmentosa (RP). Moderate to severe non-progressive high frequency hearing loss with RP and …
The Usher syndromes (US) are a group of inherited disorders that feature autosomal recessive neurosensory hearing lo …
Variations in the cochlear implant experience in children with enlarged vestibular aqueduct.
Pritchett C, Zwolan T, Huq F, Phillips A, Parmar H, Ibrahim M, Thorne M, Telian S. Pritchett C, et al. Laryngoscope. 2015 Sep;125(9):2169-74. doi: 10.1002/lary.25187. Epub 2015 Feb 3. Laryngoscope. 2015. PMID: 25647353 Free article.

A statistically significant defect-related and linguistic-status pattern was noted, impacting the timing of implantation: IEVA = 112.8 months, IP 2 = 58.4 months (P < .001), prelingual deafness = 53.8 months, postlingual deafness = 110.8 months (P < .001). Controlling for i

…
A statistically significant defect-related and linguistic-status pattern was noted, impacting the timing of implantation: IEVA = 112.8 month …
Successful cochlear implantation in prelingual profound deafness resulting from the common 233delC mutation of the GJB2 gene in the Japanese.
Matsushiro N, Doi K, Fuse Y, Nagai K, Yamamoto K, Iwaki T, Kawashima T, Sawada A, Hibino H, Kubo T. Matsushiro N, et al. Laryngoscope. 2002 Feb;112(2):255-61. doi: 10.1097/00005537-200202000-00011. Laryngoscope. 2002. PMID: 11889380
OBJECTIVES: Recently, we identified three novel mutations of the GJB2 gene in Japanese families with autosomal-recessive non-syndromic deafness.1 Seven of 11 mutated chromosomes (63.6%) contained a 233delC allele, suggesting that the 233delC mutation is the most com …
OBJECTIVES: Recently, we identified three novel mutations of the GJB2 gene in Japanese families with autosomal-recessive non-s …