1.
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
2.
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
3.
Alport's syndrome
遗传性肾炎神经性耳聋综合征;阿尔波特氏综合
4.
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
5.
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
6.
Clinical effect of the audio frequeney resonance treatment on the children with brain impair syndrome accompanied with nervous deafness.
声频共振治疗脑损伤综合征合并神经性耳聋70例疗效观察
7.
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
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.
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
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.
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
12.
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
13.
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
14.
Large Aquaeductus Vestibuli and Children Sudden Perceptive Nerve Deafness
大前庭水管综合征与儿童突发感音神经性耳聋的临床观察
15.
Hyperbaric Oxygen(HBO) Therapy of Sudden Sensorineural Deafness(SSND)
高压氧综合治疗突发性耳聋的疗效
16.
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。
17.
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
18.
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