1.
Clinical genetics and gene mapping studies on a family with autosomal dominant congenital cataract
常染色体显性遗传性白内障一家系的临床遗传学及基因定位研究
2.
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
3.
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
4.
The Study of Disease-Causing Genes of Autosomal Dominant Congenital Cataract;
常染色体显性遗传白内障致病基因的研究
5.
The Study of Causative Genes in a Chinese Family with Autosomal Dominant Congenital Cataract;
常染色体显性遗传先天性白内障一家系致病基因研究
6.
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
7.
Recent research progress of pathogenic genes in autosomal dominant hereditary pulverulent cataracts
常染色体显性遗传性粉尘状白内障致病基因的研究进展
8.
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
9.
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。
10.
Laparoscopic Management of Autosomal Dominant Polycystic Kidney;
常染色体显性遗传性多囊肾病的腹腔镜治疗
11.
With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance.
据系谱分析,该疾病符合常染色体显性遗传方式。
12.
Progress in treatment of autosomal dominant polycystic kidney disease
常染色体显性遗传多囊肾病的治疗研究进展
13.
FHCM is a heterozygote autosomal dominant disease, and the incidence rate in male is obvious higher than that in female.
属杂合子常染色体显性遗传性疾病,男性患病率高于女性。
14.
HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
HHT是常染色体显性遗传性血管发育异常的一种疾病。
15.
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
16.
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
17.
Cerebral Autosomal Dominat Arteriopathy with Subcortical Infarcts and Leukoencep-halopathy
伴有皮层下梗死和白质脑病的常染色体显性遗传性脑动脉病(附一家系临床及治疗观察)
18.
Clinical analysis of two CADASIL families
伴皮层下梗死和白质脑病的常染色体显性遗传性脑动脉病2个家系的临床分析