Six tumbrils roll along the streets.

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 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。

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）。

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

Although previous hybridization tests proved that polydactyly trait belonged with an autosomal dominant inheritance but the penetrance is difference in offspring populations.

已有杂交试验证明鸡多趾性状为常染色体显性遗传但外显率不同。

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。

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。

70 patients ( 63.6%) had positive family history and they showed mostly autosomal dominant inheritance. The rate of consanguinity was 6.9%.

有家族史者70例（63.6%），其中常染色体显性遗传17个家系，近亲结婚者5个家系（6.9%）。

The results of genetic analysis in this disease group suggest that hemochromatosis is an autosomal dominant inheritance but not autosomal recessive inheritance disease.

本组病例遗传方式分析结果，不支持常染色体隐性遗传，确定为常染色体显性遗传。

The hereditary APC-R family was identified, and it appeared to manifest autosomal dominant inheritance. 3.

确定为遗传性APC-R家系，符合常染色体显性遗传规律。

Conclusions GEFS~+ is autosomal dominant inheritance disease with conspicuous genetic heterogeneity and phenotypic heterogeneity.

结论GEFS+为常染色体显性遗传性疾病，具有显著遗传异质性和表型异质性。

RESULTS: Of the family investigated, an autosomal dominant inheritance mode with high penetrance and variable expressivity was suggested.

结果：收集的1个3代非综合征型缺牙家系符合常染色体显性遗传，疾病外显率高，但表现度极不一致。

Conclusion The depressed hypoxia response might have been influenced by genetic factors. The model was in accord with autosomal dominant inheritance.

结论低氧呼吸驱动反应性降低可能受遗传因素的影响，且遗传方式符合常染色体显性遗传；

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

结论：手掌小鱼际区真实花纹可能属于常染色体显性遗传。

The results showed that a pat ˉ tern of autosomal dominant inheritance was noticed in all three families.

结果3家系共20例患者，遗传方式均呈常染色体显性遗传；

Conclusion Genetic factors play a major role in the pathogenesis of familial gallstone disease, characterized by autosomal dominant inheritance.

结论（1）家族性胆囊结石病具有常染色体显性遗传特点，遗传因素是发病的基础。

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

结论（1）该家族呈常染色体显性遗传；

Two sensory defect congenital nystagmus families accompanying with congenital aniridia showed autosomal dominant inheritance.

2个先天性感觉缺陷性眼球震颤家系皆伴有先天性无虹膜，呈常染色体显性遗传。

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。

Approximately 2/ 3 of the patients have the family history, and follow the autosomal dominant inheritance pattern.

约2/3的患者有家族病史，表现为常染色体显性遗传，余1/3患者为散发病例。