autosomal dominant inherited disease
常染色体显性遗传病
Autosomal dominant oculocutaneous albinism
常染色体显性遗传眼皮肤白化病
This disorder is inherited as an autosomal dominant trait.
本病作为常染色体显性传递。
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
常染色体显性遗传型少汗外胚层发育不良综合征
A Family History of Vitiligo with Autosomal Dominant Inheritance
一个常染色体显性遗传白癜风家系
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。
Genetic characteristic in pedigrees of autosomal dominant hereditary hearing loss
常染色体显性遗传性耳聋家系的遗传学特征分析
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
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。
Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait.
与其它焦虑症一样, 可能作为常染色体显性性状遗传。
Clinical and pathological features of autosomal dominant inherited central core disease
常染色体显性遗传性中央轴空病的临床表现和病理特点
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。
A Sixgeneration 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？
The genetic analysis showed that this disease was caused by autosomal dominant inheritance.
遗传分析表明，该疾病属常染色体显性遗传。
Genetic Study on the Anticipation Phenomenon of Autosomal Dominant Nonsyndromic Hearing Loss
常染色体显性遗传无综合征耳聋早发现象的研究
Relationship between genotype and phenotype of autosomal dominant polycystic kidney disease.
常染色体显性遗传性多囊肾病基因型与临床表型的关系
Results The inheritance pattern of the ADAAA family was autosomal dominant with complete penetrance.
结果该家系得遗传模式为常染色体显性遗传，完全外显。
Comparison of laparoscopic and open cyst decortication for autosomal dominant polycystic kidney disease
蝮腔镜和开放去顶减压术治疗多囊肾的临床效果比较
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
Dentinogenesis imperfecta is a kind of mesodermal defect inherited in a simple autosomal dominant mode.
牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。
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。
The Positioning Study of the Pathogenic Gene Loci in a Family with Autosomal Dominant Primary Erythermalgia
一原发性红斑肢痛症家系致病基因的定位研究
Screening Results of Rhodopsin Gene Mutations in Four Chinese Autosomal Dominant Retinitis Pigmentosa Families
视紫红质基因在显性视网膜色素变性家系的突变筛查
Relationship of renal function with renal volume and renal blood flow in autosomal dominant polycystic kidney disease
常染色体显性多囊肾病肾功能与部分参数的相关性分析
The detrimental effect of urinary tract infection on renal function of adults with autosomal dominant polycystic kidney disease
成人多囊肾病泌尿系感染与肾功能损害的相关性研究
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