<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Gregor, Anne</dc:creator>
  <dc:creator>Albrecht, Beate</dc:creator>
  <dc:creator>Bader, Ingrid</dc:creator>
  <dc:creator>Bijlsma, Emilia K</dc:creator>
  <dc:creator>Ekici, Arif B</dc:creator>
  <dc:creator>Engels, Hartmut</dc:creator>
  <dc:creator>Hackmann, Karl</dc:creator>
  <dc:creator>Horn, Denise</dc:creator>
  <dc:creator>Hoyer, Juliane</dc:creator>
  <dc:creator>Klapecki, Jakub</dc:creator>
  <dc:creator>Kohlhase, Jürgen</dc:creator>
  <dc:creator>Maystadt, Isabelle</dc:creator>
  <dc:creator>Nagl, Sandra</dc:creator>
  <dc:creator>Prott, Eva</dc:creator>
  <dc:creator>Tinschert, Sigrid</dc:creator>
  <dc:creator>Ullmann, Reinhard</dc:creator>
  <dc:creator>Wohlleber, Eva</dc:creator>
  <dc:creator>Woods, Geoffrey</dc:creator>
  <dc:creator>Reis, André</dc:creator>
  <dc:creator>Rauch, Anita</dc:creator>
  <dc:creator>Zweier, Christiane</dc:creator>
  <dc:date>2011</dc:date>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/158105</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1186/1471-2350-12-106</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/issn/1471-2350</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>BMC Medical Genetics. - Springer Science and Business Media LLC. - 2011, vol. 12, no. 1</dc:source>
  <dc:title xmlns:ns0="xml" ns0:lang="en">Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
