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Related Experiment Video

Updated: Dec 15, 2025

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

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

Mutation in CEP135 causing primary microcephaly and subcortical heterotopia

Daniel Bamborschke^1,2, Hülya-Sevcan Daimagüler^1,2, Andreas Hahn³

¹Center for Molecular Medicine Cologne (CMMC), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

American Journal of Medical Genetics. Part A

|July 10, 2020

Summary

No abstract available in PubMed .

Keywords:

CEP135 neuronal migration defect primary microcephaly subcortical heterotopia

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