1 Ocak 2018 Dergi makalesi Açık Erişim

Atik, T.; Isik, E.; Ozen, S.; Akgun, B.; Onay, H.; Cogulu, O.; Erguner, B.; Savas, S.; Ozkinay, F.

Dublin Core

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  <dc:creator>Atik, T.</dc:creator>
  <dc:creator>Isik, E.</dc:creator>
  <dc:creator>Ozen, S.</dc:creator>
  <dc:creator>Akgun, B.</dc:creator>
  <dc:creator>Onay, H.</dc:creator>
  <dc:creator>Cogulu, O.</dc:creator>
  <dc:creator>Erguner, B.</dc:creator>
  <dc:creator>Savas, S.</dc:creator>
  <dc:creator>Ozkinay, F.</dc:creator>
  <dc:date>2018-01-01</dc:date>
  <dc:description>Öz bulunamadı.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/93021</dc:identifier>
  <dc:identifier>oai:zenodo.org:93021</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>EUROPEAN JOURNAL OF HUMAN GENETICS 26 480-480</dc:source>
  <dc:title>HOXC4 gene is possibly responsible for Lin-Gettig syndrome</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
</oai_dc:dc>