autosomal dominant inheritance是什么意思，autosomal dominant inheritance的意思翻译、用法、同义词、例句

常染色体显性遗传

Conclusion FC has obvious heterogeneity, and its mode of inheritance is autosomal dominant inheritance with reduced penetrance.

结论FC存在明显的遗传异质性，其遗传模式呈常染色体显性遗传伴不完全外显性。

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。

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。

Inherited style of primary hypertension was not autosomal dominant inheritance are autosomal recessive inheritance.

不属于常染色体显性或隐性遗传方式。

Herediatery nonpopsis colorectal cancer(HNPCC) is an autosomal dominant inheritance syndrome , its penetrance is as high as 70 - 80% , and occupy about 5-15% of the colorectal cancer.

遗传性非息肉病性大肠癌（HNPCC）主要与遗传因素有关，呈常染色体显性遗传，外显率高达70%-80%。

Conclusions(1) HNPCC is of autosomal dominant inheritance (AD).

结论（1 ）该家族呈常染色体显性遗传；

Owing to the influence of various complex factors, it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.

由于各种复杂因素的影响，常染色体显性遗传的杂合子有可能出现不同的表现型，本文阐述了常染色体显性遗传的几种类型。

The hereditary mode of this family line is a autosomal dominant inheritance, which differs from those which have been reported.

本家系遗传方式为常染色体显性遗传，和其它学者报告不同。

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。

Results ①Three DDEB families are in line with autosomal dominant inheritance;

结果①符合常染色体显性遗传；

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。

Conclusion The congenital cataract is the human phenotype defect caused by injured DNA. It is compatible with the autosomal dominant inheritance.

结论先天性白内障是由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。

Pedigree analysis indicated autosomal dominant inheritance.

呈常染色体显性遗传。

The results showed that 24, 51, 19, 14 epileptic families were respectively in the modes of autosomal dominant inheritance, autosomal recessive inheritance, X-sex inheritance, polygenic inheritance.

共发现24个常染色体显性遗传家系，19个X-连锁显性或隐性遗传家系，51个常染色体隐性遗传家系，另有14个家系为非孟德尔遗传模式。

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。

Conclusion:The family investigation suggested that the formation of cup ear was determined by the cup ear gene of an affected parent and it was an autosomal dominant inheritance.

所查杯状耳均无耳聋病史及其它部位畸形。结论：杯状耳的形成是由父母双方中一方杯状耳基因决定的，家系分析显示为常染色体显性遗传。

Objective: To elucidate the molecular mechanism of neurofibromatosis type 2 (NF2) with autosomal dominant inheritance disease in a Chinese kindred.

目的：探讨中国人常染色体显性遗传2型神经纤维瘤病的基因突变和分子诊断。

Result: It's autosomal dominant inheritance in this family.

结果：该家族为常染色体显性遗传家系。

The results indicate that psoriasis is of autosomal dominant inheritance and incomplete phenotype.

认为银屑病属于常染色体显性遗传，伴不全表现。

From all these characteristics autosomal dominant inheritance was unambiguously established.

上述特征完全符合常染色体显性遗传的特点。

We think that the vitiligo in the family history is caused by autosomal dominant inheritance.

作者认为该家系的白癜风为常染色体显性遗传。

The transmission accords with autosomal dominant inheritance.

符合常染色体显性遗传。

Conclusions The autosomal dominant inheritance is often incomplete. The clinical feature is often complicated as the neoplasm in the concerned glands might not develop simultaneously.

结 论此种常染色体显性遗传病可出现外显不全，所累及腺体并不同时发病使临 床症状复杂。

Conclusion :The family investigation suggested that the formation of cup-ear was determined by the cup-ear gene of an affected parent and it was an autosomal dominant inheritance.

结论 ：杯状耳的形成是由父母双方中一方杯状耳基因决定的，家系分析显示为常染色体显性遗传。

Connective tissue nevi are uncommon hamartomas that may be acquired or may manifest an autosomal dominant pattern of inheritance.

结缔组织痣是一种很少见的的错构瘤，可能与常染色体显性遗传有关。