Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review

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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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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

Joël Gambrelle1, Marianne Till, Bibi Lukusa

  • 1Department of Ophthalmology, Croix-Rousse Hospital, Lyon, France. joel.gambrelle@chu-lyon.fr

Ophthalmic Genetics
|June 15, 2007
PubMed

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