1.
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
2.
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
3.
Molecular Pathogenesis Study for an Extensive Nonsyndomic Deafness Family Associated with A1555G Mutation;
线粒体A1555G突变相关非综合征耳聋大家系的分子病因学研究
4.
Analysis of the Candidate Genes in an Autosomal Recessive Nonsyndromic Hearing Impairment Kindred;
一常染色体隐性非综合征耳聋家系的候选基因分析
5.
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
6.
GJB2 (connexin 26) gene mutation screen in patients with nonsydromic hearing loss in Hunan
GJB2基因在湖南地区非综合征耳聋患者中的突变分析
7.
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
8.
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
9.
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
10.
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
11.
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
12.
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
13.
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
14.
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
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.
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
17.
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
18.
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