autosomal dominant的例句大全

Family investigation result in, X-Chromosom sex linked inheritance dominant in 1 cases, Rarely inheritance recessive in 3 cases ( autosomal recessive inheritance in 2 case, X-chromosom sex linked recessive inheritance in 1 case), no report in china.

家系调查结果：显性遗传1例，稀有的隐性遗传3例，国内尚未见报导。

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；

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。

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。

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。

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。

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。

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。

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。

Gene mutations in human gene can cause various diseases. The human autosomal dominant brachydactyly type B ( BDB) and autosomal dominant polycystic kidney disease ( PKD) are due to gene mutation on chromosome.

人类基因组上基因的突变可以引起各种各样疾病的发生，人的常染色体显性的B型短指和常染色体显性的多囊肾综合症就是由于染色体上的基因突变引起的。

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。

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。

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

结论（1）该家族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。

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: 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。

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；