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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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X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3

Agi K Gedeon1, John Nelson, Jozef Gécz

  • 1Centre for Medical Genetics, Department of Laboratory Genetics, Women's and Children's Hospital, Adelaide, Australia.

American Journal of Medical Genetics. Part A
|July 29, 2003
PubMed

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