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

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。

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；