autosomal dominant

The inheritance pattern of EDMD includes X-linked recessive, autosomal dominant and recessive modes.

其遗传方式为X - 连锁隐性 、 染色体显性和隐性遗传.

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。

This disease for autosomal dominant inheritance, and its development and sun-related.

本病为常染色体显性遗传, 其发展与日晒有关.

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.

The ac2+-Mg2+-ATPase activity of EH patients is distinctly defective and controled by genetic factors and transmitted in autosomal dominant inheritance.

EH患者钙泵活性明显改变，受遗传因素控制，是垂直传递，为常染色体显性遗传。

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.

Sex-limited autosomal dominant inheritance

性限常染色体显性遗传；限性常染色体显性遗传

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.

Approximately 25% of all cases are probably due to genetic defects, the majority of these inherited non-syndromic cataracts show autosomal dominant inheritance ( AD);

大约25%的先天性白内障与遗传缺陷有关。遗传性先天性白内障有三种不同的遗传方式：常染色体显性遗传（AD）、常染色体隐性遗传（AR）和X连锁隐性遗传（XR）。

Autosomal dominant cutis laxa with severe lung disease: Synthesis and matrix deposition of mutant tropoelastin

常染色体显性遗传性皮肤松弛症伴重度肺部疾病：弹性蛋白原突变体的合成和基质沉积

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.

Neurofibromatosis is one of autosomal-dominant neurogenetic diseases with relatively low incidence.

神经纤维瘤病是一常染色体显性遗传性疾病,临床上较为少见.

Conclusion: EXT is an autosomal dominant disorder and the penetrance is 97 % in this report.

结论: 证实EXT为常染色体显性遗传病,本组外显率为97%.

Hereditary Non-Polyposis Colorectal Cancer Syndrome ( HNPCC ) is an autosomal dominant hereditary condition.

遗传性( 非 瘜 肉 ) 结直肠癌是一种显性的常染色体遗传病.

Multiple osteochondromas can occur either spontaneously an autosomal dominant disorder known as hereditary multiple exostoses.

多发骨软骨瘤可能是自发,也可能是常染色体显性遗传疾病—遗传性多发性外生骨疣病的表现.

Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris ( IV ) .

目的研究一常染色体显性遗传寻常型鱼鳞 病家 系的致病基因.

Familial Adenomatous Polyposis Syndrome ( FAP ) is an autosomal dominant hereditary condition.

家族性结直肠瘜肉综合症 ( FAP ) 是一种显性的常染色体遗传病.

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.

Two main modes of inheritance exist: X-linked and autosomal dominant.

本病存在两种主要的遗传方式: X - 连锁型和常染色体显性型.

This disorder is inherited as an autosomal dominant trait.

本病作为常染色体显性传递.