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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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14q12 Microdeletion syndrome and congenital variant of Rett syndrome

Maria Antonietta Mencarelli1, Tjitske Kleefstra, Eleni Katzaki

  • 1Medical Genetics, University of Siena, Siena, Italy.

European Journal of Medical Genetics
|March 24, 2009
PubMed

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