Dr Gina Gómez, from the National Autistic Society, said research into fragile X syndrome could help understanding of certain aspects of autism.
全国自闭症协会的Gina Gómez博士认为对于脆性X综合症的研究有助于理解自闭症的某些方面。
They were aggressive, slow learners, and kept convulsing in seizures-classic signs of Fragile X syndrome.
他们表现的很具有进攻性，学习缓慢，并在发作时持续抽搐——脆性X综合征的典型迹象。
Conclusion the parents with mentally retarded students knew little about the fragile X syndrome, but whose acceptability of screening was high.
结论培智学校学生家长对脆性X综合征的了解很少，但对此病的高危筛查接受性高。
Dr Gina gomez DE la Cuesta, from the National Autistic Society, said research into fragile X syndrome could help understanding of certain aspects of autism.
全国孤独症协会的GinagomezdelaCuesta博士认为对于脆性X综合症的研究有助于加深对孤独症的了解。
The PCR-Sequence gel silver staining was more rapid, immediate, simple and economy, which suits to the colony screening fragile X syndrome on a large scale.
运用PCR -序列分析胶银染法快速、直接、简便、实用，适合脆性X综合征的大规模群体筛查。
We hope and expect that, like other developmental disorders such as Fragile X syndrome, the use of mouse models will lead directly to clinical trials that can benefit patients.
我们希望并期待其他发育障碍，如x染色体脆弱症。老鼠试验能够帮助进行对有益于病人的临床试验。
Results of phenotypical, patho-psychological and molecular-genetic analysis of the 53 probands with clinical features of the fragile X syndrome and 10 female carriers are presented.
结果表型，病理心理和分子遗传学分析的53个渊源与临床特征的脆性X综合征和10名女性运营商提出。
Fragile X syndrome, a single genetic mutation on the X chromosome, is the most common source of inherited mental impairment, affecting one in every 4,000 boys and one in every 6,000 girls.
脆性X综合征，一个X染色体上的基因突变，是遗传性智力障碍最常见的来源，每4000名男孩和每6000名女孩中就有一名儿童患有该症。
Fragile X syndrome, a single genetic mutation on the X chromosome, is the most common source of inherited mental impairment, affecting one in every 4, 000 boys and one in every 6, 000 girls.
脆性X综合征，一个X染色体上的基因突变，是遗传性智力障碍最常见的来源，每4000名男孩和每6000名女孩中就有一名儿童患有该症。
Further research of this method will introduce a more simple and rapid method for detecting male patients with fragile X syndrome. This method may be used for general population screening.
这一方法的进一步研究，将使脆性X男性患者的诊断方法更加简单、快速，有可能用于大规模群体筛查。
Objective: to establish an efficient method to detect fragile X chromosome syndrome (FraX) by optimizing PCR amplifying condition.
目的：优化PCR扩增条件，建立一种有效检测脆性X综合征的方法。
Objective: to establish an efficient method to detect fragile X chromosome syndrome (FraX) by optimizing PCR amplifying condition.
目的：优化PCR扩增条件，建立一种有效检测脆性X综合征的方法。
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