1.
Mutational Analysis of Mitochondrial DNA in Familes with Maternally Inherited Hearing Loss;
母系遗传性耳聋线粒体DNA突变分析
2.
Collecting, Characterizing of the Genetic Resource and Molecular Mapping of the Relevant Genes for Hereditary Hearing Impairment;
遗传性耳聋家系的收集、保存及基因定位研究
3.
Analysis of deafness gene mutations by gene chip and its clinical significance
遗传性耳聋基因芯片检测及其临床意义
4.
SLC26A4 IVS7-2A>G gene mutation in hereditary hearing loss families
遗传性耳聋家系的SLC26A4 IVS7-2A>G基因突变分析
5.
Mapping and Cloning the Causative Genes in Chinese Pedigrees with Hereditary Hearing Loss and Molecular Epidemiology of Connexins in Sporadic Population with Hereditary Hearing Loss;
遗传性耳聋致病基因定位克隆与缝隙连接蛋白分子流行病学研究
6.
Establishment and Application of Mutation Screening System Based on DHPLC for Hereditary Deafness;
基于DHPLC的遗传性耳聋基因突变检测平台的建立和应用
7.
Conclusion These loci are the candidate positions for maternal inheritance nonsyndromic deafness.
这些位点频率较高的等位基因可能与导致母系遗传性耳聋的相关基因连锁
8.
unable to speak because of hereditary deafness.
因为遗传性的耳聋所以不能说话。
9.
Pathogeny and Therapy of a Genetic Conductive Hearing Loss Genealogy
一个遗传性传导性耳聋家系的病因及治疗
10.
Alport's syndrome
遗传性肾炎神经性耳聋综合征;阿尔波特氏综合
11.
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
12.
The electro-audiogram shows that yours is a type of nerve deafness ( conduction deafness, mixed type deafness).
您的电测听图表明是神经性耳聋（传导性耳聋，混合性耳聋）。
13.
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
14.
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
15.
Analyzing the Hereditary Features and the DNA Mutations in a Large Pedigree with Non-sensoneural Hearing Loss;
感音神经性耳聋的家系遗传学特征及基因突变分析
16.
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
17.
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
18.
Analysis of the Relatoin between Gene Mutation and Clinical Phenotype for Autosomal Recessive Families
常染色体隐性遗传耳聋家系基因突变与临床表型的研究