<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>Kause, Franziska</dc:creator>
  <dc:creator>Zhang, Rong</dc:creator>
  <dc:creator>Ludwig, Michael</dc:creator>
  <dc:creator>Schmiedeke, Eberhard</dc:creator>
  <dc:creator>Rissmann, Anke</dc:creator>
  <dc:creator>Thiele, Holger</dc:creator>
  <dc:creator>Altmueller, Janine</dc:creator>
  <dc:creator>Herms, Stefan</dc:creator>
  <dc:creator>Hilger, Alina C.</dc:creator>
  <dc:creator>Hildebrandt, Friedhelm</dc:creator>
  <dc:creator>Reutter, Heiko</dc:creator>
  <dc:date>2019</dc:date>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/92643</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/bdr2.1493</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/issn/2472-1727</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Birth Defects Research. - Wiley. - 2019, vol. 111, no. 10, p. 591-597</dc:source>
  <dc:title xmlns:ns0="xml" ns0:lang="en">HSPA6
            : A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>