1.
Molecular Genetic Analysis of Waardenburg Syndrome and Non-syndromic Hearing Loss
Waardenburg综合征和非综合征型耳聋的分子遗传学研究
2.
Molecular Mechanism of Late-onset Nonsyndromic Hearing Loss and Age-related, Aminoglycoside-induced Hearing Loss
迟发性非综合征型耳聋及老年性、药物性耳聋的分子机制研究
3.
Molecular Genetic Analysis of the Mitochondrial DNA 1555 Mutation Gene among Nonsyndromic Hearing Impairment Patients from Jilin Province;
吉林省非综合征型耳聋分子病因学分析
4.
Molecular Finding in Two Chinese Families with Nonsyndromic Hearing Impairment;
两个非综合征型耳聋家系的分子遗传学研究
5.
Mutation analysis of GJB2 gene in deaf population from Chongqing city
重庆市非综合征型耳聋患儿GJB2基因突变分析
6.
Molecular genetic analysis of the mtDNA A1555G mutation in patients with non-syndromic hearing loss
非综合征型耳聋线粒体基因A1555G突变分析
7.
The Clinical Features and Mutation Analysis of the Responsible Genes for the Syndromic Hearing Impairment;
综合征型耳聋临床表型特征分析及相关基因突变研究
8.
Study on the Mitochondrial DNA Mutation and the Phenotype Diversity of Nonsyndromic Hearing Loss;
非综合征型耳聋线粒体DNA突变及其临床表型多样性的研究
9.
Mutation Screening and Whole Spectrum Mutation Map Drawing of GJB2 Gene among Non-syndromic Hearing Impairment Patients;
非综合征型耳聋患者GJB2基因突变筛查和全频谱突变图谱绘制
10.
Association Studies on Susceptibility Loci (Gene) of Two Types of Non-syndromic Hearing Impairment;
遗传性非综合征型耳聋两种致病基因易感位点的关联分析
11.
Optimization and Application of Genetic Diagnostic System for Hereditary Nonsyndromic Hearing Loss
遗传性非综合征型耳聋基因诊断体系的优化和应用
12.
Mutation Analysis of GJB3 in HAN PEOPLE with Non-syndromic Hearing Impairment in Xinjiang
新疆地区汉族遗传非综合征型耳聋人群GJB3基因突变分析
13.
Genetic Analysis of Non-syndromic Hearing Loss and Waardenburg Syndrome;
非综合征性耳聋及Waardenburg综合征的遗传学分析
14.
Genome-Wide Scanning for a Nonsyndromic Autosomal Dominant Deafness in a Six-Generation Family;
无综合征型常染色体显性感音神经性耳聋家系的基因定位
15.
Mapping and Identified the Causative Genes in Chinese Nonsyndromic X-linked Hereditary Hearing Loss Pedigrees;
非综合征型X连锁显性遗传耳聋家系致病基因的定位及鉴定研究
16.
Alport's syndrome
遗传性肾炎神经性耳聋综合征;阿尔波特氏综合
17.
Keratitis, ichthyosis, and deafness syndrome (KID syndrome) is a rare congenital disorder disease.
目的 观察角膜炎、鱼鳞病、耳聋综合征的临床表现。
18.
Mutational analysis of SLC26A5 IVS2-2A>G in Chinese Han patients with non-syndromic hearing loss
中国汉族非综合征耳聋患者SLC26A5 IVS2-2A>G的突变