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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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Congenital heart disease affects local gyrification in 22q11.2 deletion syndrome

Marie Schaer1, Bronwyn Glaser, Meritxell Bach Cuadra

  • 1Service Médico-Pédagogique, Department of Psychiatry, University of Geneva School of Medicine, Geneva, Switzerland.

Developmental Medicine and Child Neurology
|May 7, 2009
PubMed

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