隐的例句大全

The Enshrouded Difference of Arithmetic Progression with n Order

n阶等差数列的隐蔽公差

You should tell her the truth and be done with it.

你应该告诉她真相,不要在隐瞒事实了.

And live alone in the bee-loud glade.

然后独隐在蜂吟的深处.

Han had an ashy complexion, which on a cloudy day could blend in perfectly with the color of the surrounding sky and make him invisible-a first-rate camouflage.

韩学愈容颜灰暗，在阴天可以与周围的天色和融无间，隐身不见，是头等保护色。

They live this sort of boring life where they grow and divide, and they've always been considered to be these asocial reclusive organisms.

它们的生活好像只是单调乏味的成长与分裂，而且长久以来被认为是不善社交的隐居生命体。

Idea for Establishing the Provincial Assessment Center of Risk Sources and Hidden Dangers

建立省级危险源及隐患评估中心的构想

In electronic commerce protocols for transactions of physical goods, three properties are needed: security, atomicity, and privacy.

面向物理商品交易的电子商务协议需要具备3个属性：安全、原子和隐私。

I will keep back nothing from you.

我对你什么都不隐瞒.

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。

The Proportion and Clinical Feature of Duchenne Muscular Dystrophy With Autosomal Recessive Inheritance

常染色体隐性遗传的类Duchenne肌营养不良临床特征及其发生比率的估计值分析

Objective To explore the clinical features of autosomal recessive juvenile Parkinson disease ( AR-JP).

目的探讨常染色体隐性遗传性青少年型帕金森病（AR-JP）的临床特征。

Wilson ′ s disease is a autosomal recessive inherited disease characteristic by metabolic disorder of copper.

肝豆状核变性是一种铜代谢障碍的常染色体隐性遗传病。

Autosomal recessive polycystic kidnay disease: clinical, pathological and radiological correlations

常染色体隐性遗传性多囊肾病：临床、病理与影像学表现

The recurrence risk for this disease is, of course, 25% because of the autosomal recessive inheritance pattern.

因为它是常染色体隐性遗传的，所以它在家族中的发病率是25%。

Citrin deficiency is inherited in an autosomal recessive manner.

希特林缺乏综合征是一种常染色体隐性遗传性疾病。

Parkin is a causative gene of autosomal recessive juvenile parkinsonism.

Parkin是隐性遗传性少年型帕金森病的致病基因。

A study of DJ-1 gene in 3 pedigrees with autosomal recessive early-onset Parkinson's disease

常染色体隐性遗传早发型帕金森病家系的DJ-1基因研究

Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation

伴共济失调和智力发育迟缓的常染色体隐性遗传的进行性肌阵挛性癫痫

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；

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。