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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
08:22

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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Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe

Mustafa Ghanim1, Sylvie Rossignol, Bruno Delobel

  • 1Centre de Référence Anomalies du Développement et Syndromes Malformatifs Nord de France, CHRU Lille, France. mustafa.ghanim@najah.edu

American Journal of Medical Genetics. Part A
|February 13, 2013
PubMed

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