期刊
NEUROLOGY
卷 65, 期 9, 页码 1496-1498出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/01.wnl.0000183066.09239.b6
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资金
- NCRR NIH HHS [5 M01 RR-01271] Funding Source: Medline
- NINDS NIH HHS [NS01692] Funding Source: Medline
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.
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