A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene; mandibulofacial disostosis, guion-almeida type
dc.contributor.author | Gerik-Çelebi, B | |
dc.contributor.author | Ceylaner, S | |
dc.contributor.author | Çam, S | |
dc.date.accessioned | 2025-04-10T10:30:17Z | |
dc.date.available | 2025-04-10T10:30:17Z | |
dc.identifier.e-issn | 1476-5438 | |
dc.identifier.issn | 1018-4813 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14701/36909 | |
dc.language.iso | English | |
dc.title | A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene; mandibulofacial disostosis, guion-almeida type | |
dc.type | Meeting Abstract |