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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

新生儿听力筛查
Newborn Hearing Screening

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临床医学进展Vol.12 No.2, 全文下载: PDF HTML XML DOI:10.12677/ACM.2022.122160, February 18 2022

耳穴注射治疗突发性耳聋的95例分析
Analysis of 95 Cases of Sudden Deafness Treated by Auricular Point Injection

傅 俊, 陈少辉, 吴玲玲   

中医学Vol.10 No.4, 全文下载: PDF HTML XML DOI:10.12677/TCM.2021.104064, June 30 2021

《二十四史》及《清史稿》罕见性遗传性相关疾病考
A Study on Rare Genetic Diseases Historically Reviewed in 24 Ancient History Books and Historical Manuscripts of Qing Dynasty

林乔   

亚洲遗传病病例研究Vol.1 No.2, 全文下载: PDF HTML DOI:10.12677/ACRG.2013.12003, May 8 2013

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Study on the Value of Oral Chinese Medicine in Reducing ABO Hemolysis of Newborn in Pregnant Women with Blood Type O

邹 芳, 程平平, 祝 佩, 黄 艳, 严丽丽    科研立项经费支持

中医学Vol.12 No.7, 全文下载: PDF HTML XML DOI:10.12677/TCM.2023.127274, July 31 2023

扩展性携带者筛查的应用与挑战
Applications and Challenges of Expanded Carrier Screening

马 君, 师娟子, 屈鹏飞   

临床医学进展Vol.12 No.9, 全文下载: PDF HTML XML DOI:10.12677/ACM.2022.1291194, September 9 2022