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Updated: Aug 16, 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

CDG-Id caused by homozygosity for an ALG3 mutation due to segmental maternal isodisomy UPD3(q21.3-qter)

E Schollen1, S Grünewald, L Keldermans

  • 1Center for Human Genetics, UZ Leuven, Leuven, Belgium. Els.Schollen@uz.kuleuven.ac.be

European Journal of Medical Genetics
|August 2, 2005
PubMed

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