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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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Global distribution of the most prevalent deletions causing hypotonia-cystinuria syndrome

Kevin Martens1, Inge Heulens, Sandra Meulemans

  • 1Laboratory for Biochemical Neuro-endocrinology, Department for Human Genetics, University of Leuven and Flanders Interuniversity Institute for Biotechnology, Gent, Belgium

European Journal of Human Genetics : EJHG
|June 21, 2007
PubMed

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