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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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Neurological manifestations of 2q31 microdeletion syndrome

Nobuhiko Okamoto1, Sadami Kimura2, Keiko Shimojima3

  • 1Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.

Congenital Anomalies
|February 2, 2017
PubMed

Keywords:
2q31 microdeletion syndromeHOXDZNF385Bintellectual disability

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