1Deafness Genetic Testing-an Example of Translational Medicine Accelerating the Progress of OtologyYUAN Yongyi, DAI Pu1-52Clinical Application of DNA microarray in rapid genetic diagnosis of non-syndromic heaing lossWANG Guojian, ZHANG Guanbin, YUAN Yongyi, HUANG Shasha, LI Yuanyuan, KANG Dongyang, CHENG Jing, DAI Pu6-103Model Evaluation and Discussion in Rehabilitation and Prevention for Hereditary Deaf FamilyHAN Mingyu, LU Yanping, BIAN Xuming, WANG Longxia, HUANG Shasha, WANG Guojian, KANG Dongyang, ZHANG Xin, DAI Pu11-144Clinical diagnosis and genetic testing for Pendred syndromeYUAN Yongyi, HUANG Shasha, ZUO Lujie, ZHANG Guozheng, DAI Pu15-185Prevalence of SLC26A4 mutations in deafness with unilateral enlarged vestibular aqueduct syndromeHUANG Shasha, HUANG Bangqing, DONG Min, MENG Xiaoxiao, DAI Pu19-226The analysis of Cytogenetics microarray screening in patients with non-syndromic Enlarged Vestibular AqueductZHAO Jiandong, YUAN Yongyi, WANG Guojian, HUANG Shasha, DAI Pu23-257Pathogenic analysis of a novel mutation of deafness gene SLC26A4GAO Xue, XIN Feng, YUAN Huijun, DAI Pu26-298Study on the Relationship between the Pathogenic Mutations of GJB2、SLC26A4 and CT Phenotypes of Inner Ear in Patient with Sensorineural Hearing LossSUN Baochun, DAI Zhiyao, HUANG Shasha, HAN Bing, YUAN Yongyi, SU Yu, KANG Dongyang, DAI Pu30-339Audiological Features/Genotype Correlations in GJB2 MutationDAI Zhiyao, SUN Baochun, HUANG Shasha, KANG Dongyang, ZHANG Xin, DONG Min, YUAN Yongyi, DAI Pu34-3610The use of genetic testing in infants who do not pass the neonatal hearing screeningLI Qi, SONG Jianmin, LIU Yaqing, FANG Ruping, DAI Pu37-4011Gene diagnosis in patients with Kartagener syndrome induced chronic secretory otitis mediaZHANG Jing, BAI Yin, YOU Shaohua, JI Lingchao, JIA Jingjie, QUE Xin, XU Cong, WANG Hongtian41-4412Targeted gene capture and massively parallel sequencing to identify causative genes mutations in clinical genetic testing for hereditary hearing lossSU Yu, TANG Wenxue, DAI Zhiyao, GAO Xue, WANG Guojian, HUANG Shasha, KANG Dongyang, LIN Xi, DAI Pu45-4913Heteroplasmy Levels of Mitochondrial 12S rRNA A1555G Mutation in Pedigrees with Aminoglycoside-Induced and Non-Syndromic Hearing Loss as Detected Using SNaPshot TechniqueZHU Yuhua, ZHAI Suoqiang, DAI Pu50-5314Detection of GJB2 Gene Sequence Length in Patients with Nonsyndromic Deafness and Monoallelic GJB2 Gene MutationsWANG Huibing, YU Fei, DAI Pu, SHAN Xizheng, YUAN Yongyi, ZHANG Xin, KANG Dongyang, HAN Dongyi54-5615A novel POU3F4 gene mutation for X-linked recessive hereditary hearing lossHUANG Bangqing, ZENG Jialing, SU Yu, HUANG Shasha, YUAN Yongyi, WANG Guojian, ZHAO Hui, DAI Pu57-6016Clinical and genetic features of a large Chinese family with nonsydromic autosomal dominant hearing lossZHANG Xiuju, CHENG Jing, LU yu, WANG Yanfei, ZHANG Lei, YUAN Huijun, HAN Dongyi61-6717Clinical and Molecular Diagnosis in Two Chinese Families with Enlargement of Vestibular AqueductTIAN Xiaoli, CUI Shuping, DUAN Naichao, MA Jiangang, JIANG Xinxia, HUANG Aiping, LIU Yanping, ZHU Qingwen68-7118Construction and Management of a Clinical Deafness Gene Diagnosis LaboratoryKANG Dongyang, HUANG Shasha, YUAN Yongyi, DAI Pu72-7619The experiment research of the Piezosurgery in temporal bone surgeryFeng Guodong, Tian Xu, Gao Zhiqiang86-8920Auricle reconstruction of microtiaSU Faren, DING Jinghua, BO Lin, LIU Xingang90-92 