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- fra X chromosome syndrome 脆性X染色体综合征
- macrotestis labeled X chromosome syndrome 巨睾丸标记X染色体综合征
- fragile X chromosome(fra X) 脆性X染色体
- fragile X chromosome syndrome 脆性X染色体综合征
- The proband of pedigree A with highexpression of fragile X chromosome(35/273) was detected to be a full mutation patient of fragile X syndrome by the molecular genetic test. A家系先证者脆性X染色体高表达（35/273），分子遗传学检查证实为脆性X综合征全突变患者；
- In women, a faulty gene on one X chromosome is counteracted by a healthy copy. 对女性而言，那条正常X染色体上的基因完全可以替代另一条X染色体上的异常基因。
- If we change the X chromosome to "Y" by bombarment method (or something like that). 如果我们用方法，将X染色体的其中一段打断，变成"Y";染色体。
- The cloned retinoschisis gene (RS1) maps to the distal short arm of the X chromosome (Xp22.2). 近年来的研究已将RS基因定位于Xp22.;2(X染色体短臂远端)。
- DMD occurs when a gene on the X chromosome fails to make the essential muscle protein dystrophin. 这种疾病的病因是在X染色体上的一个基因不能表达抗肌肉萎缩蛋白。
- A noncoding gene named Xist produces an active RNA that coats the unneeded X chromosome. 称为Xist的非编码基因制造了活性RNA，将不必要的X染色体给覆盖起来。
- But many primates, including humans, hae a third photopigment, encoded by a second gene on the X chromosome. 但是多数灵长类包括人类有着三种感光色素，通过在X染色体中的第二种基因编码。
- Rather, we happened to find something on the X chromosome," Dr.Younkin explained. 相反的，我们碰巧在X染色体发现一些东西。
- In the article, we used PCR - gel elec-trophoresis method to determine the number of repeat of P(CGG) n. We have 126 normal X chromosomes and 18 X chromosomes obtained from fra (X)families. 采用PCR凝胶电泳法测定126条正常人群X染色体及来源于脆性X综合征家族的18条染色体的P(CGG)n重复数目。
- In some women, most often black women, the two X chromosome each encode a different G6PD isoenzyme. 在一些妇女，特别是黑人妇女，两条x染色体各自编码一种不同的G6PD同工酶。
- Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes? 光敏感性癫痫在男性较少见是否由于X染色头感光色素基因变异?
- X-linked agammaglobulinemia is a genetic disease linked to the X chromosome and is seen in very young children. “一样的花费，更好的质量和服务”，这是新华翻译社对客户的承诺。
- But many primates, including humans, have a third photopigment, encoded by a second gene on the X chromosome. 但是多数灵长类包括人类有着三种感光色素，通过在X染色体中的第二种基因编码。
- There is random inactivation of one X chromosome in all cells of the female embryo at the blastocyst stage. 在胚泡期，女性的胚胎所有的细胞中，任意一条x染色体将失活。
- Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype. 目的探讨X-连锁迟发性脊椎骨骺发育不良(SEDL)基因逃避X染色体失活(XCI)及与临床表型的关系。
- Apoptosis inducing factor(AIF), whose gene lies in X chromosome, is likely an apoptogenic effector protein to mediates nuclear apoptosis directly. 凋亡诱导因子 (apoptosis inducingfactor ;AIF)基因定位于X染色体上 ;其编码产物是一种可直接介导细胞核凋亡的效应分子 .
