Analysis of non-syndromic hearing loss caused by splicing abnormalities due to a synonymous mutation of MYO15A gene in a Chinese populationWANG Si-ji, GUO Yi-lian, ZHONG Ming-jun421-426
Identification of a novel NOG gene mutation in a pedigree having stapes ankylosis with broad thumbs and toes and analysis of the clinical manifestationsZAHNG Zhao, LU Yu, YANG Chang-liang427-431
Genetic diagnosis of autosomal recessive deafness caused by rare homozygous mutation of ESPN gene and evaluation of cochlear implant rehabilitation outcomesLIU Yan, ZHONG Ming-jun, XIONG Wen-yu432-436
Analysis on the characteristics of common deafness gene mutations in congenital deafness patients and their family members in Guangxi regionLIN Zuan-ping, YUN Lu, GAN Han-xiao437-441
A study on the mutations of mitochondrial gene 12S rRNA among Zhuang people with normal hearing in Guangxi regionZHANG Shao-jie, TANG Feng-zhu, WANG Rong442-446
Experimental observation on the effect of sodium salicylate enhancing oxidative stress-mediated injury of cochlear spiral ganglion neuronsZHU Xiao-ting, HUANG Jia-lin, LIN Xiao-yu447-451
Analysis on the influence of total ear reconstruction operation of congenital malformation of external and middle ear on children's depression tendencyWENG Jin, XU Jia-jie, SUN Yi452-456
Assessment of survival prognosis after radical hepatectomy in non-hepatitis B associated with hepatocellular carcinoma patients by using modified albumin-bilirubin gradingLIU Hong-jun, DONG Xiao-feng, HUANG Wei457-461
Analysis of influencing factors of prognosis of patients with gallbladder cancer after radical resection and con- struction and validation of the nomogram for survival predictionWEI Zhen-kang, SHAO Feng, HUANG Qiang462-467
myeloid leukemia and its impacts on serum levels of MMP-2, SALL4 mRNA and AGPWANG Hui, LI Yan-chun, GAO Qiu-ying468-473
