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- autosomal abnormalities 常染色体异常
- Nevoid basal cell carcinoma syndrome is a rare autosomal dominant genetic disorder characterized by developmental abnormalities and tumorigenesis. 痣样基底细胞癌综合征是一种罕见的常染色体显性遗传病,以发育异常和肿瘤发生为主要临床特征。
- Fanconi anemia(FA) is a rare autosomal recessive di sorder characterized clinically by congenital abnormalities, progressive bone ma rrow failure and cancer susceptibility. Fanconi氏贫血是一种罕见的常染色体隐性遗传性疾病,表现为进行性骨髓衰竭、先天性骨骼畸形和易患癌症等。
- Retinochoroidal colobomas are rare congenital abnormalities caused by incomplete closure of the embryonic fissure.Inheritance may be autosomal dominant. 摘要先天性视网膜脉络膜缺损是一种罕见的自体显性遗传疾病，导因为胎儿时期胚胎期裂隙愈合不良所造成。
- Such abnormalities can be prevented. 这类不正常现象是可以预防的。
- The chest X-ray reveals no abnormalities. 胸部X光检查结果正常。
- A routine scan revealed abnormalities in the fetus. 一次常规扫描发现胎儿畸形。
- This disorder is inherited as an autosomal dominant trait. 本病作为常染色体显性传递。
- Dermoid sinus is a genetic, autosomal skin condition in dogs. 皮窦是一种犬类的常染色体遗传病。
- Xeroderma pigmentosum is an autosomal recessive disease. 着色性干皮病是一种常染色体的退行性疾病。
- 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。
- And immune abnormalities related to belong to autoimmune diseases. 与机体的免疫学异常有关，是属于自身免疫性疾病。
- Certain autosomal translocations in the heterozygous state can be fully viable. 呈杂合子状态的某些常染色体易位完全可以生活的。
- A routine scan revealed abnormalities in the foetus. 一次常规扫描发现胎儿畸形。
- Coronary artery fistulas are uncommon abnormalities. 摘要冠状动脉娄管是罕见的冠状动脉异常。
- Results: The proportion of autosomal structure abnormalities was 5.1% (23/454) among the patients with idiopathic oligospermia and azoospermia, while that of chromosomal polymorphism was 8.8%(40/454). 结果在454例特发性生精异常患者中有23(5.;1%25)例涉及常染色体结构异常;40(8
- 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。
- Other cloned animals had been found to have high rates of abnormalities. 克隆动物出现畸形和异常的几率相当高。
- 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。
