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基因微阵列分析可以鉴别胼胝体异常患者的候选位点
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作者 Sherr E.H. owen r. +1 位作者 Albertson D.G. 陈海 《世界核心医学期刊文摘(神经病学分册)》 2006年第3期32-33,共2页
Absence of the corpus callosum is often associated with cognitive deficits, autism, and epilepsy. Using a genomic microarray, the authors analyzed DNA from 25 patients with radiographically confirmed callosal anomalie... Absence of the corpus callosum is often associated with cognitive deficits, autism, and epilepsy. Using a genomic microarray, the authors analyzed DNA from 25 patients with radiographically confirmed callosal anomalies and identified three patients with de novo copy number changes in chromosome regions 2q37, 6qter, and 8p. Chromosomal deletions and duplications may be a relatively common cause of cerebral malformations. 展开更多
关键词 基因微阵列 候选位点 脑发育畸形 孤独症 认知功能 染色体丢失 影像学 缺如 拷贝数
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