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
血液流变学在突聋治疗中的研究进展Advances in Hemorheology in the Treatment of Sudden Sensorineural Hearing Loss
崔琬苓, 蒋路云, 廖林志, 张 淇, 王 玲, 熊彦青, 谢 艳 科研立项经费支持
临床医学进展Vol.14 No.12, 全文下载: PDF XML DOI:10.12677/acm.2024.14123230, December 30 2024
耳蜗电图及其在突发性聋中的应用Electrocochleogram and Its Application in Sudden Sensorineural Hearing Loss
王玉霞, 宋志民
临床医学进展Vol.11 No.11, 全文下载: PDF HTML XML DOI:10.12677/ACM.2021.1111712, November 3 2021
中国西南地区肺癌患者基因突变特点及其与临床特征的相关性分析Characteristics of Gene Mutations in Lung Cancer Patients in Southwest China and Analysis of Their Correlation with Clinical Features
牟 康, 沈依帆, 李小松
临床医学进展Vol.15 No.1, 全文下载: PDF XML DOI:10.12677/acm.2025.151147, January 22 2025
基于叶绿体基因组变异位点的百合属(百合科)植物资源遗传多样性的分子鉴定新方法A Novel Method for Molecular Identification of Genetic Diversity of Plant Resources in Lilium L. (Liliaceae) Based on Taxon-Specific Variable Nucleotide Characters from Whole Chloroplast Genome Sequences
刘美辰, 刘一心, 左云娟, 靳晓白, 杨志荣, 索志立
植物学研究Vol.13 No.4, 全文下载: PDF XML DOI:10.12677/br.2024.134050, July 30 2024
一例非特异性精神发育迟滞家系OPHN1基因突变分析并文献复习Genotype Analysis of OPHN1 Gene Mutation in Non-Specific Mental Retardation Family with Literature Review
段会坤, 王 莉, 胡 爽, 白周现, 孔祥东 科研立项经费支持
临床医学进展Vol.10 No.1, 全文下载: PDF HTML XML DOI:10.12677/ACM.2020.101001, January 6 2020