1 Ocak 2022 Dergi makalesi Açık Erişim

Vargel, Ibrahim; Canter, Halil Ibrahim; Kucukguven, Arda; Aydin, Asim; Ozgur, Figen

Dublin Core

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  <dc:creator>Vargel, Ibrahim</dc:creator>
  <dc:creator>Canter, Halil Ibrahim</dc:creator>
  <dc:creator>Kucukguven, Arda</dc:creator>
  <dc:creator>Aydin, Asim</dc:creator>
  <dc:creator>Ozgur, Figen</dc:creator>
  <dc:date>2022-01-01</dc:date>
  <dc:description>Aim: The term frontonasal dysplasia (FND) represents a spectrum of anomalies and its genetics have not been well defined. Recently, the critical role of the aristaless-like homeobox (ALX) gene family on the craniofacial development has been discovered. In the present study, we aimed to propose a systematic surgical treatment plan for the ALX-related FNDs according to the genotypic classification as well as demonstrating their clinical characteristics to help surgeons diagnose the underlying pathology accurately.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/233554</dc:identifier>
  <dc:identifier>oai:aperta.ulakbim.gov.tr:233554</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>CLEFT PALATE-CRANIOFACIAL JOURNAL 59(5) 637-643</dc:source>
  <dc:title>ALX-Related Frontonasal Dysplasias: Clinical Characteristics and Surgical Management</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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