在线字典为您在线查询常体的词典内容如下，包括常体的拼音，读音，拼读；常体的意思和详细释义，常体的近反义词，常体的英语翻译，用常体这个词语怎么造句等内容。
常体读音/繁体/五笔/英文翻译
| 拼音 | cháng tǐ | 读音 | 跟我读 |
|---|---|---|---|
| 繁体 | 常體 | 类型 | 词语大全 |
| 五笔 | 此词无五笔连打 | 平音 | changti |
| 词性 | 中性 | 语法 | |
| 拼读 | 吃(chi1)昂(ang2)，常(chang2)|特(te1)蚁(yi3)，体(ti3) | ||
| 英语翻译 | 正常体温normal body temperature;[生理]normothermia |
常体是什么意思？
· 基本释义
1.犹通例。 《荀子·荣辱》：“乐易者常寿长，忧险者常夭折，是安危利害之常体也。”《后汉书·邓张徐张胡传论》：“怀禄以图存者，仕子之恒情；审能而就列者，出身之常体。”《魏书·食货志》：“输京之时，听其即纳，不得杂合，违失常体。”
2.固定的格式。《南史·张邵传》：“夫文岂有常体，但以有体为常。”
3.平素的风格。唐 殷璠《河岳英灵集》卷中 崔颢 诗评语：“顥 年少为诗，名陷轻薄，晚节忽变常体，风骨凛然，一窥塞垣，説尽戎旅。”
· 详细释义
犹通例。
《荀子·荣辱》：“乐易者常寿长，忧险者常夭折，是安危利害之常体也。”《后汉书·邓张徐张胡传论》：“怀禄以图存者，仕子之恒情；审能而就列者，出身之常体。”《魏书·食货志》：“输京之时，听其即纳，不得杂合，违失常体。”
固定的格式。
《南史·张邵传》：“夫文岂有常体，但以有体为常。”
平素的风格。
唐 殷璠 《河岳英灵集》卷中 崔颢 诗评语：“ 顥 年少为诗，名陷轻薄，晚节忽变常体，风骨凛然，一窥塞垣，説尽戎旅。”
· 网络释义
常体，汉语拼音cháng tǐ ㄔㄤˊ ㄊㄧˇ，出自《荀子·荣辱》。
常体的近反义词？
常体近义词：抱歉，查无常体的近义词
常体反义词：抱歉，查无常体的反义词
常体词语接龙
（~常体~）在开头的接龙：体育，体温，体操，体面，体魄，体谅，体恤，体裁，体重，体校，体罚，体制，体系，体坛，体能，体力，体检，体癣，体积，体格
（~常体~）在结尾的接龙：物体，全体，字体，通体，躯体，媒体，液体，得体，流体，个体，人体，颜体，形体，胶体，整体，天体，繁体，国体，球体，本体
暂时无法为您进行常体的词语顺序接龙!
用常体怎么造句？
您好，暂未查询到常体造句的内容。
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。
The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
她抛弃了小说新手常走的老路，没有采用同情心洋溢的半自传体，这本身就值得称道。
That she departs from the route of sympathetic semi-autobiography used by most first-time novelists is itself worthy of praise.
如果我们在课常上以堕胎展开辩论，有些人可能会说，“胎儿是有知觉的生命体，所以它有生存的权利，它的母亲不应该扼杀它”。
If we have a debate about abortion in this class, people — some people might say, "Look. The fetus is a sentient being and as such it has a right to survive and shouldn't be killed by its mother."
属于或关于常染色体的。
Of or relating to an autosome.
由于常染色体上出现突变基因而导致的疾病。
A disease caused by the presence of two recessive mutant genes on an autosome.
小细胞癌常无明显的大核仁（而恶性黑色素瘤常有），偶尔伴有核内假包涵体。
Small cell carcinomas usually do not show large prominent nucleoli, whereas melanomas often do, accompanied by occasional intranuclear pseudoinclusions.
遗传性嗜中性白血球减少症是一种常染色体隐性遗传疾病，该疾病导致成体中性粒细胞无法从骨髓迁移到血液中。
Trapped Neutrophil Syndrome is an autosomal recessive disease which results in mature neutrophils being unable to migrate from the bone marrow into the blood.
获取一类闭于光照鲁棒的、具无颜色恒常性功能的颜色描述女闭于齐部盘算机视觉体解来道长短常从要的。
To get a color descriptor that is robust to illumination and has the color constancy function is very important for the entire computer vision system.
皮窦是一种犬类的常染色体遗传病。
Dermoid sinus is a genetic, autosomal skin condition in dogs.
钢衬塑运输槽罐的钢体部分的制作，按照JB/T4735-1997《钢制焊接常压容器》标准。
Transport steel tanks lined with plastic body parts of the steel production, in accordance with the JB/T4735-1997 "welded steel pressure vessel" standard.
目的研究常染色体显性遗传型多囊肾病肾组织中细胞外基质和多囊蛋白-1的表达及与囊肿发生的关系。
Objective To study the expression of extracellular matrix and polycystin-1 in ADPKD and their relation to cyst formation.
聋哑是常染色体隐性遗传病，通过遗传分析发现，减少或防止近亲结婚可以降低聋哑人的出生。
It is a recessive hereditary disease of autosome to be deaf and dumb. it was analysed through heredity that reducing or preventing consanguineous marriage can reduce the deaf-mute's birth rate.
可以发现退行性椎体滑移常出现在椎体滑移、椎管狭窄以及节段性不稳的分类中，这说明了它的临床表现是多种多样的。
DS can be found in classifications of spondylolisthesis, spinal stenosis, and segmental instability, indicating that the clinical presentation is varied.
该方法为常染色体显性多囊肾疾病行胚胎植入前遗传学诊断提供了依据。
It provide an evidence of using this technique for the PGD for ADPKD.
结果显示各类序列的进化水平沿常染色体呈现明显的非均匀性和规律性。
The results show that the evolution levels of each kind of sequences along chromosomes take on obvious heterogeneity and regularity.
在雌性个体中，遗传功能失活的晚复制x染色体淡染色，可以和常染色体以及另一条X染色体鉴别。
In female individuals a late replicating X chromosome which genetically was inactive slightly stained and could be discriminated from the autosomes and other X chromosome.
脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。
Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.
目前根据遗传方式分为1型（常染色体显性）和2型（常染色体隐性） ，每一型根据不同基因缺陷又分为许多亚型。
The limb-girdle muscular dystrophies are divided into two types according to inheritance pattern, type 1 is autosomal dominant and type 2 is autosomal recessive.
首先，本工作开发了一基团贡献模型用于预测常压下聚合物熔体的导热系数。
The first one is a group contribution model for the prediction of the thermal conductivity of polymer melts.
结果：146例外周血染色体异常核型中常染色体数目异常占4.8％（7/146）； 常染色体结构异常占29.5％（43/146）；
Results: In 146 cases of chromosomes aberrance, the rate of abnormal eu-chromosome number and abnormal euchromosome structure was 4. 8% (7/146) and 29. 5% (43/146).
受损害的组织、衰老的木材和离层下方的位置常发现侵填体，这可以完全阻塞负责运输的导管系统。
Tyloses are often found in injured tissue, older wood, and below an abscission layer , and can completely block the conducting vessel.
目的：研究华东地区汉族人常染色体显性遗传性多囊肾病(adpkd)基因型与临床表现型的关系。
Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.
目的探讨卡马西平睡前一次用药治疗常染色体显性遗传夜间额叶癫(adnfle)患儿的疗效及其与生物节律的关系。
Objective to study the effect of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) with carbamazepine being taken at a draught before sleep and its relationship with biological rhythm.
所查杯状耳均无耳聋病史及其它部位畸形。结论：杯状耳的形成是由父母双方中一方杯状耳基因决定的，家系分析显示为常染色体显性遗传。
Conclusion:The family investigation suggested that the formation of cup ear was determined by the cup ear gene of an affected parent and it was an autosomal dominant inheritance.
结论原发性高血压是由DNA损伤引起的人类表型缺陷，该病症符合常染色体显性遗传，具延迟外显性。
Conclusion: the essential hypertension is the human phenotype blemish caused by injured DNA. It is compatible with an autosomal dominant inheritance and its performance is delayed.
方法：筛选出患长qt综合征1型的家庭成员，并鉴定KCNQ1基因中一个常染色体显性遗传突变基因(R190 Q)。
Methods We screened a family affected by long-QT syndrome type 1 and identified an autosomal dominant missense mutation (R190Q) in the KCNQ1 gene.
胱氨酸病是以常染色体隐性方式遗传。
Genetic counseling. Cystinosis is inherited in an autosomal recessive manner.
胱氨酸病是以常染色体隐性方式遗传。
Genetic counseling. Cystinosis is inherited in an autosomal recessive manner.
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