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

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。

The transmission accords with autosomal dominant inheritance.

符合常染色体显性遗传。

Results The mode of inheritance conforms to autosomal dominant inheritance and polygenic inheritance.

结果遗传方式符合常染色体显性遗传及多基因遗传方式。

Conclusion: The mode of inheritance of SEDC may be autosomal dominant inheritance.

结论：SEDC遗传方式为常染色体显性遗传。

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。

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 genetic analysis shows it is autosomal dominant inheritance.

遗传学分析结果显示该家系的遗传方式符合常染色体显性遗传规律。

It is obviously autosomal dominant inheritance according to the pedigree.

由于第一代病例仅为右眼虹膜缺损，故较支持中胚层迷走发育的理论。

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

结果①符合常染色体显性遗传；

They are going to remove into a new building.

他们准备搬进一幢新楼.

They're going to remove into a new building.

他们准备搬进一座新楼.

Usually, it is better not remove out outer leaves from fruits and vegetables before storage.

通常最好不要在冷藏前剥去水果和蔬菜上的叶子.

These circumstances are complained finally company of card remove furniture, make its incur injustice.

这些情况最后都投诉到正牌搬场公司, 使其蒙受不白之冤.

It is a common occurrence in dogs and is thought to be a sex-limited autosomal recessive trait.

该疾病常发于犬，并被认为具有限性常染色体隐性遗传特征。

Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.

脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。

WD is a common autosomal recessive inherited neuropathy, whose only pathogenic gene is ATP7B.

WD是神经科较为常见的常染色体隐性遗传病，其唯一致病基因为ATP7B基因。

Multiple carboxylase deficiency ( MCD) is an autosomal recessive disorder of inherited metabolic diseases.

多种羧化酶缺陷症（MCD）是一种常染色体隐性遗传的先天遗传代谢性疾病。

The results of segregation analysis indicate that the genetic pattern of UU multiplex families and UA group is autosomal recessive.

分离分析结果显示，U×U多发家庭组和U×A家庭组可以接受常染色体隐性遗传的假设；