1.
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
2.
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
3.
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
4.
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
5.
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
6.
sex-limited autosomal dominant inheritance
性限常染色体显性遗传;限性常染色体显性遗传
7.
Mutation screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa with conformation-sensitive gel electrophoresis
运用构象敏感凝胶电泳筛查常染色体显性视网膜色素变性患者视紫红质基因突变的研究
8.
The Study of Loca lization of Autosomal Dominant Retinitis Pigmentosa Gene and Detection of Mutation on Rhodopsin Gene
常染色体显性视网膜色素变性基因定位的研究与视紫红质基因突变的检测
9.
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
10.
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
11.
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
12.
Screening for Causing Genes in Autosomal Dominant Retinitis Pigmentosa
显性视网膜色素变性致病基因的筛查
13.
According to genetic analysis, this disease is caused by autosomal dominant inheritance.
经过遗传分析，认为该畸形属常染色体显性遗传。
14.
Missense mutation in the βB1-crystallin gene caused autosomal dominant congenital cataract in China
晶状体蛋白βB1基因错义突变引起常染色体显性遗传性白内障
15.
Candidate Gene Screening for Autosomal Dominant Auditory Neuropathy in a Chinese Pedigree;
常染色体显性遗传性听神经病家系候选基因突变筛查
16.
Genetic Mapping and Mutation Analysis in Chinese Family with Congenital Cataract;
单纯常染色体显性遗传性白内障致病基因的定位及突变研究
17.
Screening Mutation of Related Genes in a Family with Autosomal Dominant Genetic Pulverulent Cataract
常染色体显性遗传性粉尘状白内障一家系的相关基因突变筛查
18.
MYP2 Gene Mapping of Autosomal Dominant High Myopia in Chinese Families;
常染色体显性遗传高度近视家系MYP2基因定位分析