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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 submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations

Irina Balikova1, Thomy de Ravel, Carmen Ayuso

  • 1Centre for Human Genetics, University Hospitals Leuven, Katholieke Universiteit Leuven, Leuven, Belgium.

American Journal of Ophthalmology
|March 1, 2011
PubMed
Abstract

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