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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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Genetic Overlap between Holoprosencephaly and Kallmann Syndrome

K Vaaralahti1, T Raivio, R Koivu

  • 1Institute of Biomedicine/Physiology, University of Helsinki, Finland.

Molecular Syndromology
|August 3, 2012
PubMed

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