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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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Neurogenic arthrogryposis multiplex congenita and velopharyngeal incompetence associated with chromosome 22q11.2

Manuel Castro-Gago1, José Mariá Iglesias-Meleiro, Manuel Oscar Blanco-Barca

  • 1Departamento de Pediatría, Servicio de Neuropediatría, Hospital Clínico Universitario, Universidad de Santiago de Compostela, Spain. pdcastro@usc.es

Journal of Child Neurology
|March 29, 2005
PubMed

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