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- autosomal dominant ichthyosis vulgaris 常染色体显性遗传寻常型鱼鳞病
- Mapping of Pathogenic Genes in a Pedigree with Autosomal Dominant Ichthyosis Vulgaris 一常染色体显性遗传寻常型鱼鳞病家系致病基因的定位
- autosomal dominant ichthyosis 常染色体显性的干皮病
- This disorder is inherited as an autosomal dominant trait. 本病作为常染色体显性传递。
- Tuberous sclerosis (TSC) is a common autosomal dominant disease. 结节性硬化症是一种临床较常见的显性遗传病。
- ichthyosis vulgaris autosomal dominant 常染色体显性遗传寻常型鱼鳞病
- 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。
- It is obviously autosomal dominant inheritance according to the pedigree. 由于第一代病例仅为右眼虹膜缺损，故较支持中胚层迷走发育的理论。
- The Alzheimer in this ancestry appears as autosomal dominant genetic disease. 阿尔茨海默病在本家系中显示为常染色体显性遗传。
- 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。
- A Six-generation Family with Autosomal Dominant Deafness Passed Along: Possibly A New Locus? 六代相传显性遗传耳聋大家系:一个可能的新基因座?
- Objective: To study the effects of rhodopsin (RHO) gene in autosomal dominant retinitis pigmentosa (adRP). 摘要目的：探讨视紫红质基因在视网膜色素变性疾病中的作用。
- Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before. 神经纤维瘤病，以前又称von Recknn沙ausen病，属常染色体显性遗传病。
- Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode. 摘要牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。
- Peutz-Jeghers, also known as Hereditary Intestinal Polyposis Syndrome, is an autosomal dominant genetic disease. 什么是'黑斑息肉综合征-多生长在肠道'?
- Objective To analyze the occurrence character of autosomal dominant familial polycystic kidney. 目的分析常染色体显性遗传多囊肾的发病特点。
- 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。
- Conclusion The congenital teeth agenesis maily is autosomal dominant inheritant disease. 结论先天缺牙家系多为常染色体显性遗传；
- It can be autosomal dominant, autosomal recessive, or X-linked mode of inheritance. 他可以是体染色体显性、体染色体隐性、或是性联遗传等方式的遗传疾病。
- Dentin dysplasia is a genetic disorder of teeth, commonly exhibiting an autosomal dominant inheritance. 什麽是'牙本质发育异常-牙本质发育异常'?
