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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual

C Windpassinger1, E Petek, K Wagner

  • 1Institute of Medical Biology and Human Genetics, and University Clinic for Ophthalmology, University of Graz, Austria.

Clinical Genetics
|April 19, 2003
PubMed

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