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Updated: Jul 18, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

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

Ocular findings in the chromosome 22q11.2 deletion syndrome

Brian J Forbes1, Gil Binenbaum, Jane C Edmond

  • 1Division of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA. forbesb@email.chop.edu <forbesb@email.chop.edu>

Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|December 5, 2006
PubMed
Abstract

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