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- autosomal dominant aniridia 常染色体显性无虹膜
- 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。
- 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'?
- Some members of the patient s family were similarly affected and indicated an autosomal dominant trait of inheritance. 一些亲属亦有类似病症，显示是体显性遗传模式。
- Objective A case of Autosomal dominant pigmentary type of orthochromatic leukodstrophy(POLD) was reported. 目的探讨显性遗传性色素颗粒型正染性脑白质营养不良的临床和病理改变特点。
- As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant. 家族性腺瘤息肉病的遗传方式是常染色体显性遗传。
