<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>Nikopoulos K</dc:creator>
  <dc:creator>Butt GU</dc:creator>
  <dc:creator>Farinelli P</dc:creator>
  <dc:creator>Mudassar M</dc:creator>
  <dc:creator>Domènech-Estévez E</dc:creator>
  <dc:creator>Samara C</dc:creator>
  <dc:creator>Kausar M</dc:creator>
  <dc:creator>Masroor I</dc:creator>
  <dc:creator>Chrast R</dc:creator>
  <dc:creator>Rivolta C</dc:creator>
  <dc:creator>Siddiqi S</dc:creator>
  <dc:date>2016</dc:date>
  <dc:identifier>https://sonar.ch/global/documents/293991</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1111/cge.12645</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/26285675</dc:relation>
  <dc:source>Clinical genetics. - 2016</dc:source>
  <dc:title xmlns:ns0="xml" ns0:lang="en">A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>