Autosomal英文翻译_含义_读音_Autosomal例句

It is usually inherited as an autosomal dominant trait, although autosomal recessive and X-linked inheritance are seen less commonly.

人群中，大部分遗传性白内障是外显率较高的常染色体显性遗传，但也有X连锁和常染色体隐性遗传存在。

Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.

儿童型脊髓性肌萎缩症是常见的遗传性神经肌肉病，为常染色体隐性遗传。

Multiple osteochondromas can occur either spontaneously or in an autosomal dominant disorder known as hereditary multiple exostoses .

多发骨软骨瘤可能是自发，也可能是常染色体显性遗传疾病—遗传性多发性外生骨疣病的表现。

They also found adermatoglyphia to be autosomal dominant, meaning only one parent needs to pass on the mutation for the child to show it.

他们也发现皮纹病是显性遗传，意味着只有一个父母将突变传给孩子去显现出来。

Genetic analysis indicated that the CVD character is controlled by an autosomal recessive gene with 100% penetrance.

遗传分析表明，心血管疾病的性质是由一个常染色体隐性基因外显率100%。

An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.

除了正常染色体对以外，还存在有第二种同源染色体的非整倍体状态，被称为三体性。

This type of inheritance is called autosomal recessive inheritance.

这种被称为常染色体隐性遗传继承。

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。

Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait.

与其它焦虑症一样，可能作为常染色体显性性状遗传。

Objective: To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes.

目的：探讨常染色体隐性遗传性共济失调家系的临床特征并排除已知的致病基因。

ABSTRACT: Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris (IV).

摘要：目的研究一常染色体显性遗传寻常型鱼鳞病家系的致病基因。

Recent studies have revealed mechanistic parallels between imprinted X-chromosome inactivation and autosomal imprinting.

最近的研究表明机械相似之处印迹X染色体失活和常印记。

Two rare, inherited forms have been reported in cattle, both characterized by autosomal recessive transmission.

两个少见的遗传形式报告了牛，这两个特点是常染色体隐性传染。

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。

Von Hippel-Lindau (VHL) disease is an autosomal, dominantly inherited, tumour syndrome.

希佩尔一林道（VHL）病是一种常染色体，显性遗传，肿瘤综合征。

Dense incisors (din) is a new autosomal recessive mutation in the mouse that interferes with complete eruption of the incisors.

密集切牙（标准）是一种新的常染色体隐性基因突变的老鼠会干扰完成爆发门牙。

Certain autosomal translocations in the heterozygous state can be fully viable .

呈杂合子状态的某些常染色体易位完全可以生活的。

Some members of the patients family were similarly affected and indicated an autosomal dominant trait of inheritance.

一些亲属亦有类似病症，显示是体显性遗传模式。

Congenital adrenal hyperplasia is a genetic disorder transmitted by autosomal recessive pattern.

先天性肾上腺增生症是一种自体隐性遗传病。

Results The inheritance pattern of the ADAAA family was autosomal dominant with complete penetrance.

结果该家系的遗传模式为常染色体显性遗传，完全外显。

Genetic counseling and ANKRD26 mutation analysis should be offered to patients with autosomal-dominant thrombocytopenia.

而且，也应向常染色体显性血小板减少证患者提供遗传咨询和进行ANKRD26突变分析。

After full investigation of available data a suspected autosomal dominant inheritance pattern of PS could not be confirmed.

经充分调查后对现有数据怀疑常染色体显性遗传模式的PS都没有得到证实。

Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).

目的确定常染色体显性遗传视网膜色素变性家系的致病基因及其突变位点，并研究其临床表型。

Objective To analyze the occurrence character of autosomal dominant familial polycystic kidney.

目的分析常染色体显性遗传多囊肾的发病特点。

Harlequin ichthyosis (HI)is a severe subtype of autosomal recessive congenital ichthyoses (ARCI).

丑角样鱼鳞病是常染色体隐性遗传性鱼鳞病的一种严重亚型。

The condition is passed along genetically as an autosomal dominant trait.

条件是家族的遗传作为常染色体显性遗传特征。

Autosomal trisomy is a common cause of human miscarriage, malformations and learning disability.

常染色体是人类的共同事业流产，畸形和学习障碍。

CBAS usually occurred by autosomal recessive inheritance, due to various enzymes defect in bile acid synthesis.

CBAS多属于常染色体隐性遗传，由胆汁酸合成过程中的酶缺陷所致。

The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.

该病属常染色体隐性遗传，与X-染色体关联，所以，母亲是基因携带者的男性表现为发病。

This disorder is inherited as an autosomal dominant trait .

本病作为常染色体显性传递。

常染色体的

adj.