<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>Allali, S.</dc:creator>
  <dc:creator>Le Goff, C.</dc:creator>
  <dc:creator>Pressac-Diebold, I.</dc:creator>
  <dc:creator>Pfennig, G.</dc:creator>
  <dc:creator>Mahaut, C.</dc:creator>
  <dc:creator>Dagoneau, N.</dc:creator>
  <dc:creator>Alanay, Y.</dc:creator>
  <dc:creator>Brady, A. F.</dc:creator>
  <dc:creator>Crow, Y. J.</dc:creator>
  <dc:creator>Devriendt, K.</dc:creator>
  <dc:creator>Drouin-Garraud, V.</dc:creator>
  <dc:creator>Flori, E.</dc:creator>
  <dc:creator>Genevieve, D.</dc:creator>
  <dc:creator>Hennekam, R. C.</dc:creator>
  <dc:creator>Hurst, J.</dc:creator>
  <dc:creator>Krakow, D.</dc:creator>
  <dc:creator>Le Merrer, M.</dc:creator>
  <dc:creator>Lichtenbelt, K. D.</dc:creator>
  <dc:creator>Lynch, S. A.</dc:creator>
  <dc:creator>Lyonnet, S.</dc:creator>
  <dc:creator>MacDermot, K.</dc:creator>
  <dc:creator>Mansour, S.</dc:creator>
  <dc:creator>Megarbane, A.</dc:creator>
  <dc:creator>Santos, H. G.</dc:creator>
  <dc:creator>Splitt, M.</dc:creator>
  <dc:creator>Superti-Furga, A.</dc:creator>
  <dc:creator>Unger, S.</dc:creator>
  <dc:creator>Williams, D.</dc:creator>
  <dc:creator>Munnich, A.</dc:creator>
  <dc:creator>Cormier-Daire, V.</dc:creator>
  <dc:date>2011</dc:date>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/186132</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1136/jmg.2010.087544</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/issn/0022-2593</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Journal of Medical Genetics. - BMJ. - 2011, vol. 48, no. 6, p. 417-421</dc:source>
  <dc:subject xmlns:ns0="xml" ns0:lang="en">Genetics(clinical)</dc:subject>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Genetics</dc:subject>
  <dc:title xmlns:ns2="xml" ns2:lang="en">Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
