A Chinese treatment outcome evaluation system for cochlear implantationsCAO Yong-mao, TAO Ze-zhang, MAO Zong-fu, HUA Qing-quan, WU Zhan-yuan, YIN Li, LONG Mo, XI Xin, LIU Sha, ZHANG Qiu, HUANG Yong-lan, ZHOU Zong-kui, LI Jun, CHANG Wei, ZHU Su-qin363-367
An evaluation system for factors influencing children's rehabilitation results from cochlear implantationCAO Yong-mao, TAO Ze-zhang, MAO Zong-fu, HUA Qing-quan, WU Zhan-yuan, YIN Li, LONG Mo, XI Xin, LIU Sha, ZHANG Qiu, HUANG Yong-lan, ZHOU Zong-kui, LI Jun, CHANG Wei, ZHU Su-qin368-371
Cochlear implantation in deaf children with central nervous system diseasesXIE Li, HUA Qing-quan, CAO Yong-mao372-375
Cochlear implants in patients with long time post-lingual total deafnessLI Jia-nan, HAN Dong-yi, HONG Meng-di, CHEN Ai-ting, XI Xin, YANG Shi-ming376-381
Sequence analysis of total mitochondrial genome in a pedigree with aminoglycoside-induced hearing lossCHEN Yu-qing, LI Hai-feng, LU Ya-jie, CHEN Zhi-bin, WEI Qin-jun, CAO Xin, XING Guang-qian382-386
SOX10 gene mutation screening in one Chinese family with Waardenburg syndrome type 2CHEN Yan, FENG Yong, YANG Bai-qiu387-391
Prevalence of common genetic mutations in 839 patients with severe and profound hearing lossWANG Guo-jian, YUAN Yong-yi, HAN Bing, HUANG Sha-sha, KANG Dong-yang, ZHANG Xin, DONG Min, HAN Dong-yi, DAI Pu392-396
Frequency of gap junction beta-2 gene mutation in neonates with congenital cytomegatovirus infectionLI Lu-quan, YU Jia-lin, TAN Jun-jie, ZHOU Yuan397-401
Mitochondrial DNA 1555G mutation detection and haplotype analysis in pedigrees with deafnessLIU Chang, GAO Guo-Feng, HU Yu-hua, ZHANG Ruan-zhang, XU Zhi-yong, SONG Jun-yan, Wang Sha-yan402-406
Molecular etiology analysis among students with profound hearing loss in a special education school in ShandongJIA Jing-jie, YUAN Yong-yi, DAI Pu, WANG Guo-jian, GOU Hong-liang, XU Jian-feng, CHEN Xue-song, KANG Dong-yang, ZHANG Xin, WANG Hong-tian407-410