autosomal的例句大全

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。

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。

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%）。

Osteogenesis imperfecta ( OMIM 166200) is an autosomal dominant disorder characterized by bone fragility and abnormalities of connective tissue.

成骨不全病（OMIM166200）是一种常染色体显性遗传病，其临床表现以骨折及结缔组织异常为特征。

Van der Woude syndrome ( VWS, OMIM 119300) is an autosomal dominant craniofacial disorder characterized by pits of the lower lip, hypodontia and cleft lip and/ or cleft palate.

范德伍兹综合征（Van der Woude syndrome，VWS，OMIM119300）是一种常染色体显性遗传病。其特征是家族性下唇瘘复合唇裂或腭裂，1／4的患者伴有缺牙（Hypodontia）。

Background Familial benign chronic pemphigus or Hailey-Hailey disease ( HHD; OMIM 169600) is a rare autosomal dominant cutaneous disorder characterized by recurrent vesicles and erosions mainly in intertriginous areas.

研究背景：家族性慢性良性天疱疮，又称Hailey-Hailey病（HHD，OMIM169600）是一种罕见的常染色体显性遗传性皮肤病。

Objective To map the virulence gene for a family with coronary autosomal dominant congenital cataracts ( ADCC ).

目的初步定位具有花冠状表型的常染色体显性遗传性先天性白内障一家系的致病基因.

Hepatolenticular degeneration ( HLD ) is an autosomal reoessively inherited disease caused by copper metabolic dysfunction.

肝豆状核变性 ( Hepatolenticulardegeneration,HLD ) 是一种铜代谢紊乱而引起的常染色体隐性遗传的疾病.

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。

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。

Autosomal dominant cutis laxa with severe lung disease: Synthesis and matrix deposition of mutant tropoelastin

常染色体显性遗传性皮肤松弛症伴重度肺部疾病：弹性蛋白原突变体的合成和基质沉积

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。