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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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1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotype

Olaug K Rødningen1, Trine Prescott, Ann-Sofie Eriksson

  • 1Department of Medical Genetics, Ullevål University Hospital, Oslo, Norway. olaug.rodningen@klinmed.uio.no

European Journal of Medical Genetics
|August 30, 2008
PubMed

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