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 | 2024-07-18T11:51:37Z | |
| dc.date.available | 2024-07-18T11:51:37Z | |
| dc.identifier.issn | 1018-4813 | |
| dc.identifier.other | 1476-5438 | |
| dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/5001 | |
| dc.language.iso | English | |
| dc.publisher | NATURE PUBLISHING GROUP | |
| 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 |