1.
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
2.
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
3.
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
4.
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
5.
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
6.
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
7.
Alport's syndrome
遗传性肾炎神经性耳聋综合征;阿尔波特氏综合
8.
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
9.
The Study of the Deafness Gene GJB2 Mutation in a Hereditary Nonsyndromic Deaf Families;
遗传性非综合征性耳聋一家系人群GJB2基因突变的研究
10.
Mutation analysis of GJB3 between Chinese and Uighur population with nonsyndromic hearing impairment
GJB3基因在新疆维汉两民族遗传性非综合征耳聋患者的突变分析
11.
Gene Localization and a Novel Mutation Identified for Non-syndromic Hearing Loss;
常染色体显性遗传非综合症型耳聋基因的定位与突变筛查
12.
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
13.
Molecular Mechanism and Functional Characterization Associate with Maternally Inherited Aminoglycoside-induced and Nonsyndromic Deafness;
母系遗传药物性聋与非综合征性聋的分子遗传机制与功能研究
14.
Clinical character and etiological study of a large family with maternally inherited non-syndromic deafness
一母系遗传非综合征耳聋大家系的临床特征和病因学研究
15.
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
16.
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
17.
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
18.
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