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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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Phaeochromocytoma and paraganglioma: next-generation sequencing and evolving Mendelian syndromes

Eamonn R Maher1

  • 1Department of Medical Genetics, University of Cambridge, Addenbrooke's Treatment Centre, Cambridge; Department of Clinical Genetics, Cambridge University Hospitals, Cambridge erm1000@medschl.cam.ac.uk.

Clinical Medicine (London, England)
|August 8, 2014
PubMed
Abstract

No abstract available in PubMed .

Keywords:
DNA sequencinggeneticsparagangliomaphaeochromocytoma

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