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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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Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac

E Morava1, K E Jackson, F Tsien

  • 1University Medical Center Nijmegen, Department of Pediatrics, Nijmegen, Netherlands. emorava@cukz.umcn.nl

Genetic Counseling (Geneva, Switzerland)
|January 22, 2005
PubMed

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