autosomal dominant inheritance的意思|示意
常染色体显性遗传
autosomal dominant inheritance的网络常见释义
常染色体显性遗传 ...病的发生主要受一对等基因控制，它们的遗传方式遵循孟德尔遗传律包括：①常染色体显性遗传（autosomal dominant inheritance AD）:一种遗传性状或遗传病有关的基因位于常染色体上，其性质是显性的，这种遗传方式称为常染色体显性遗传；如脊髓小脑共济失调②常染...
常染色体显形 ... dominant - 显性的，优势的 autosomal dominant inheritance - 常染色体显形 Dominant allele - 显性等位基因 ...
包括常染色体显性遗传 ...其分为三种主要遗传方式：①常染色体遗传（autosomal inheritance）中又包括常染色体显性遗传（autosomal dominant inheritance，AD）和 ；②X 伴性遗常染色体隐性遗传（autosomal recessive inheritance，...
常染色体显形遗传 ... autosampler 自动进样器 autosomal dominant inheritance 常染色体显形遗传 autosomal inheritance 常染色体遗传 ...
autosomal dominant inheritance相关短语
1、 male-limited autosomal dominant inheritance 或为男性
2、 AD autosomal dominant inheritance 常染色体显性遗传
3、 autosomal dominant inheritance AD 常染色体显性遗传
autosomal dominant inheritance相关例句
Conclusion: the essential hypertension is the human phenotype blemish caused by injured DNA. It is compatible with an autosomal dominant inheritance and its performance is delayed.
结论原发性高血压是由DNA损伤引起的人类表型缺陷，该病症符合常染色体显性遗传，具延迟外显性。
Hereditary hemorrhagic telangiectasia is an uncommon autosomal dominant inheritance disease. 25 cases from a family were reported. The pathology, clinical presentation and treatment were discussed.
遗传出血性毛细血管扩张症为常染色体显性遗传病，临床少见，本文就其病理变化、临床特点进行讨论，探讨其治疗方法。附一家系25例分析。
The limb-girdle muscular dystrophies are divided into two types according to inheritance pattern, type 1 is autosomal dominant and type 2 is autosomal recessive.
目前根据遗传方式分为1型（常染色体显性）和2型（常染色体隐性） ，每一型根据不同基因缺陷又分为许多亚型。
At present, three modes of inheritance are identified including maternal uniparental disomy for chromosome 7 and autosomal dominant or autosomal recessive inheritance.
目前研究发现此病有三种遗传方式：即母源第7号染色体单亲双体、常染色体显性遗传及常染色体隐性遗传。
An investigation of a genetic Blepharostenosis family was reported. It was proved that the disease was congenital eyelid syndrome and autosomal dominant inheritance.
报道了一个遗传性小眼症家系的调查结果，该家系属于先天性睑裂狭小综合症，为常染色体显性遗传。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天性小眼球是一种先天发育异常性眼科疾病，遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。