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TranslationMobile

x染色體易裂癥
x染色易裂癥
脆性x染色體綜合征
脆性x染色體綜合癥
七、脆性x綜合征
染色體綜合征

"fragile" in Chinese : adj. 1.脆的，易碎的。 2.脆弱的，虛弱的。短語(yǔ) ...
"x" in Chinese : vt. (x-ed, x'd x-ing, x'ing) ...
"syndrome" in Chinese : n. 1.【醫(yī)學(xué)】綜合癥，癥候群。 2.(某一事物的)全 ...
"fragile x chromosome syndrome" in Chinese : 脆性x染色體綜合征
"fragile x chromosome" in Chinese : 脆x染色體; 脆Ｘ染色體; 脆染色體; 脆性x染色體
"fragile x mental retardation" in Chinese : 脆性x智力低下; 脆性x綜合征
"fragile x-associated mental retardation" in Chinese : 脆性x連鎖智力低下
"x syndrome" in Chinese : 愛(ài)克斯綜合征
"fragile x site induced breaking point" in Chinese : 脆性x斷點(diǎn)
"fragile" in Chinese : adj. 1.脆的，易碎的。 2.脆弱的，虛弱的。 fragil ...
"five x syndrome" in Chinese : 五x綜合征
"marker x syndrome" in Chinese : 標(biāo)志x染色體綜合征
"multiple-x syndrome" in Chinese : 多x綜合征
"poly x syndrome" in Chinese : 多x綜合征
"poly x-chromosomal syndrome" in Chinese : 多x染色體綜合征

Examples

The screnning and prenatal gene dignosis for fragile x syndrome using pfu dna
綜合征的篩查和產(chǎn)前基因診斷
Fragile x syndrome ( fxs ) is the most common form of inherited mental retardation after down syndrome . it affects approximately 1 in 4000 males and 1 in 8000 females in the general population
脆性x綜合征( fragilexsyndrome ， fxs )是導(dǎo)致遺傳性智力低下的主要原因之一，發(fā)病率僅次于先天愚型，在男性中的發(fā)病率約為1 / 4000 ，在女性中發(fā)病率約為1 / 8000 。
To detect the patients and carriers of the fragile x syndrome , various analytic methods could be used . one is cytogenetic diagnosis to observe the expression of the fragile site fraxa located at xq27 . 3
對(duì)脆x綜合征的診斷，可以通過(guò)細(xì)胞遺傳學(xué)方法觀察分析x染色體相應(yīng)脆性位點(diǎn)的表達(dá)情況，或是通過(guò)southern印跡雜交的方法直接分析cgg重復(fù)的擴(kuò)增突變。
The absence of the fmr1 gene product , fragile x mental retardation protein ( fmrp ) , is believed to be responsible for the typical physical and mental characteristics of the fragile x syndrome . alleles with between 43 and 200 cgg repeats are called permutation . they are generally unmethylated with normal transcript and protein level , but are extremely unstable during transmission to next generation
帶有前突變( n = 43 200 )的個(gè)體其fmr1基因通常不會(huì)甲基化，可以正常轉(zhuǎn)錄和翻譯產(chǎn)生fmrp ，故沒(méi)有臨床表型出現(xiàn)，但是，在向下一代傳遞的過(guò)程中卻是非常不穩(wěn)定的，會(huì)從前突變擴(kuò)增成為全突變。