Deafness Genetic Testing-an Example of Translational Medicine Accelerating the Progress of OtologyYUAN Yongyi, DAI Pu1-5
Clinical 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 Pu6-10
Model 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 Pu11-14
Clinical diagnosis and genetic testing for Pendred syndromeYUAN Yongyi, HUANG Shasha, ZUO Lujie, ZHANG Guozheng, DAI Pu15-18
Prevalence of SLC26A4 mutations in deafness with unilateral enlarged vestibular aqueduct syndromeHUANG Shasha, HUANG Bangqing, DONG Min, MENG Xiaoxiao, DAI Pu19-22
The analysis of Cytogenetics microarray screening in patients with non-syndromic Enlarged Vestibular AqueductZHAO Jiandong, YUAN Yongyi, WANG Guojian, HUANG Shasha, DAI Pu23-25
Pathogenic analysis of a novel mutation of deafness gene SLC26A4GAO Xue, XIN Feng, YUAN Huijun, DAI Pu26-29
Study 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 Pu30-33
Audiological Features/Genotype Correlations in GJB2 MutationDAI Zhiyao, SUN Baochun, HUANG Shasha, KANG Dongyang, ZHANG Xin, DONG Min, YUAN Yongyi, DAI Pu34-36
The use of genetic testing in infants who do not pass the neonatal hearing screeningLI Qi, SONG Jianmin, LIU Yaqing, FANG Ruping, DAI Pu37-40