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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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Monosomy 1p36--a recently delineated, clinically recognizable syndrome

M Zenker1, O Rittinger, K P Grosse

  • 1Institut für Humangenetik der Universität Erlangen-Nürnberg, Germany. martin.zenker@kinder.imed.uni-erlangen.de

Clinical Dysmorphology
|February 2, 2002
PubMed

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