高危新生儿听力和聋病易感基因联合筛查临床研究A Clinical Study of Hearing Concurrent Genetic Screening in High-Risk Newborns
张 章, 戴怡蘅, 李振安, 余凤慈, 刘 莹
生物医学Vol.5 No.2, 全文下载: PDF HTML XML DOI:10.12677/HJBM.2015.52003, May 28 2015
COL4A5基因新无义突变致Alport综合征一家系并文献复习A Family with Alport Syndrome Caused by a New Nonsense Mutation of COL4A5 Gene and Literature Review
王加兰, 王大海, 江世璇, 常 红
临床医学进展Vol.12 No.7, 全文下载: PDF HTML XML DOI:10.12677/ACM.2022.127940, July 15 2022
UCP3基因新突变致非综合征性肥胖的特征分析Characteristic Analysis of Non-Syndromic Obesity Caused by a New Mutation in the UCP3 Gene
汪 澍, 贾明睿, 左 玲
临床医学进展Vol.13 No.7, 全文下载: PDF HTML XML DOI:10.12677/ACM.2023.1371503, July 7 2023
针灸为主治疗突发性耳聋的研究现状Research Status of Sudden Deafness Mainly Treated with Acupuncture and Moxibustion
高 畅, 郭 静, 赵东雪, 杨博翔
临床医学进展Vol.14 No.1, 全文下载: PDF HTML XML DOI:10.12677/ACM.2024.141146, January 22 2024
PUF60基因变异致Verheij综合征一例并文献复习PUF60 Gene Mutation Caused Verheij Syndrome in a Case and Literature Review
李文颖
临床医学进展Vol.11 No.3, 全文下载: PDF DOI:10.12677/ACM.2021.113147, March 15 2021
突发性耳聋患者的前庭功能改变研究进展Research Progress on Vestibular Function Changes in Patients with Sudden Deafness
肖雨薇, 白 忠
临床医学进展Vol.14 No.7, 全文下载: PDF XML DOI:10.12677/acm.2024.1472068, July 18 2024