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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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High frequency of rare copy number variants affecting functionally related genes in patients with structural brain

Roxana Kariminejad1, Allan Lind-Thomsen, Zeynep Tümer

  • 1Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran.

Human Mutation
|September 2, 2011
PubMed

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