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.

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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。

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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.

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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.

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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。

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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.

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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

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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.

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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）。

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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

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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.

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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.

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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%.

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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.

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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.

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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.

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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.

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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.

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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.

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This disorder is inherited as an autosomal dominant trait.

本病作为常染色体显性传递.

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