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软骨发育不全

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Methods. The records of 48 of 103 children with achondroplasia seen between 1997 and 2005 were examined.

调查了1997至2005年间103名软骨发育不全患者中的48人的病历。

I am an achondroplasia dwarf, which is a person having very short limbs.

我是一名软骨发育不全的矮人,腿极短。

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。

Twenty-five cases of achondroplasia followed for a period of recent three years are reviewed.

我们分析在3年中遇到的25例软骨发育不全侏儒。

Genetic counselling and the management of complications in achondroplasia are important.

对於软骨发育不全侏儒患者的遗传谘询以及其并发症的处理是很重要的。

Of or relating to achondroplasia.

属于或关于软骨发育不全的。

The teenager, who is the world's smallest girl according to the Indian Book of Records, has a form of dwarfism called achondroplasia.

根据印度的纪录,这个十几岁的小女孩是世界上个子最小的女孩,患有一种叫做软骨发育不全的侏儒症。

The children of a person who has achondroplasia have a 50% hance of inheriting the condition;75% of people with achondroplasia are born to parents who do not have the condition.

软骨发育不全症患者的后代有50%的几率会继承这种疾病状况,75%的软骨发育不全症患者的父母没有这种疾病状况。

Objective To evaluate whether mutation in the exon 10 of the fibroblast growth factor receptor 3(FGFR3) gene in common in Chinese patients with achondroplasia.

目的 了解中国人软骨发育不全患者成纤维细胞生长因子受体3(fibroblast growth factor receptor 3,FGFR3)基因变异情况。

Improper development of cartilage at the ends of the long bones,result in g in a form of congenital dwarfism.

软骨发育不全在骨头尾部的软骨的不正常发育,从而引起先天性侏儒症

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代表父目录,所以这个命令就是执行当前目录下的"toolchain.sh"。

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