英语词汇“achondroplasia”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

软骨发育不全；

英英释义

achondroplasia[ ei,k?ndr?u'pleizi? ]

n.an inherited skeletal disorder beginning before birth; cartilage is converted to bone resulting in dwarfism
同义词：achondroplastyosteosclerosis congenitachondrodystrophy

学习怎么用

双语例句

用作名词(n.)

Like most achondroplasia dwarfs, I have two average-height parents, as well as an average-height brother.
像大多数患有软骨发育不全症的侏儒一样，我的父母身高正常，我的兄弟也很正常。
Energetic as Wan-yu is, she suffers from achondroplasia and is destined never to grow to an average size.
尽管婉榆活泼好动，她却患有软骨发育不全症，注定无法长到正常人的身高。

权威例句

Achondroplasia.
Achondroplasia.
[ACHONDROPLASIA]
Achondroplasia is defined by recurrent G380R mutations of FGFR3.
Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.
Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficien...
The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, ...

单词	achondroplasia
释义	achondroplasia 听听怎么读英 [e??k?ndr?'ple???] 美 [e??k?ndr?'ple???] 是什么意思 n. 软骨发育不全；英英释义 achondroplasia[ ei,k?ndr?u'pleizi? ] n.an inherited skeletal disorder beginning before birth; cartilage is converted to bone resulting in dwarfism 同义词：achondroplastyosteosclerosis congenitachondrodystrophy 学习怎么用双语例句用作名词(n.) Like most achondroplasia dwarfs, I have two average-height parents, as well as an average-height brother. 像大多数患有软骨发育不全症的侏儒一样，我的父母身高正常，我的兄弟也很正常。 Energetic as Wan-yu is, she suffers from achondroplasia and is destined never to grow to an average size. 尽管婉榆活泼好动，她却患有软骨发育不全症，注定无法长到正常人的身高。权威例句 Achondroplasia. Achondroplasia. [ACHONDROPLASIA] Achondroplasia is defined by recurrent G380R mutations of FGFR3. Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficien... The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, ...
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