1.
Analyzing and Mapping the Disease Gene for Two Hereditary Nonsyndromic Retinitis Pigmentosa Families;
两个遗传性非综合征型视网膜色素变性家系的基因突变检测及定位
2.
Progress in the gene-related study on autosomal retinitis pigmentosa
常染色体遗传型视网膜色素变性相关基因的研究进展
3.
Clinical and hereditary study of a family with primary retinitis pigmentosa combined with myopia
视网膜色素变性合并近视家系的临床及遗传学研究
4.
Molecular Genetics Study of Primary Retinitis Pigmentosa among Chinese;
原发性视网膜色素变性疾病的分子遗传学研究
5.
The Molecular Genetics Research of Two Retinitis Pigmentosa Pedigrees
两个视网膜色素变性家系的分子遗传学研究
6.
Genetics analysis and gene diagnosis of Chinese family with autosomal dominant retinitis pigmentosa
视网膜色素变性家系遗传分析及基因诊断
7.
Analysis of the mutations of rhodopsin gene in autosomal dominant retinitis pigmentosa family
常染色体显性遗传视网膜色素变性家系视紫红质基因突变分析
8.
Analysis of Clinical Features and Study of Responsible Genes for the Chinese Retinitis Pigmentosa and Usher Syndrome Families;
原发性视网膜色素变性家系和Usher综合征家系临床表型分析及致病基因研究
9.
Mutation Analysis of Retinitis Pigmentosa I Gene in Chinese Patients with Autosomal Dominant Retinitis Pigmentosa
常染色体显性遗传视网膜色素变性家系视网膜色素变性1基因（RP1）的突变分析
10.
Linkage Mapping of the Two Chinese Family with Autosomal Dominant Retinitis Pigmentosa;
两个常染色体显性遗传视网膜色素变性家系连锁分析
11.
Study on RP1 Gene Mutation in Chinese ADRP Patients and Assessment of Local Retinal Function of ADRP Patients with mfERG;
中国人常染色体显性遗传视网膜色素变性RP1基因突变及多焦视网膜电图研究
12.
Retinitis pigmentosa (RP) is a common genetic eye disease affecting about 1 in 3500 people worldwide with pan-ethnic occurrence.
视网膜色素变性(RP)是遗传性致盲眼病,其患病率约为1/3500。
13.
The Molecular Mechanism of Retinal Degeneration and the Therapeutic Effects of EGb761 on This Disease;
遗传性视网膜色素变性的分子机制及金纳多的治疗作用
14.
Investigation on Genetic Linkage Analysis of X-linked Retinitis Pigmentosa Using Microsatellite Markers;
应用微卫星多态位点对X连锁型视网膜色素变性疾病进行遗传连锁分析的研究
15.
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
16.
A study of retinal papilla by acquired immunodeficiency syndrome
获得性免疫缺陷综合征视网膜血管性病变
17.
The observation of ERG in patients with retinitis pigmentosa
视网膜色素变性患者视网膜电图观察
18.
Fluorescent Typing of Fundus Oculi Lesion in Primary Retinal Pigment Degeneration
原发性视网膜色素变性眼底血管荧光造影分型