| dc.contributor.author | Guzoglu, Nilufer | |
| dc.contributor.author | Aslan, Mustafa K. | |
| dc.contributor.author | Gunay, Yasemin D. | |
| dc.contributor.author | Atasoy, Pinar | |
| dc.contributor.author | Ceylaner, Serdar | |
| dc.contributor.author | Aliefendioglu, Didem | |
| dc.date.accessioned | 2021-01-14T18:10:32Z | |
| dc.date.available | 2021-01-14T18:10:32Z | |
| dc.date.issued | 2020 | |
| dc.identifier.citation | Bu makale açık erişimli değildir. | en_US |
| dc.identifier.issn | 0962-8827 | |
| dc.identifier.issn | 1473-5717 | |
| dc.identifier.uri | https://doi.org/10.1097/MCD.0000000000000317 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12587/12657 | |
| dc.description | WOS:000545915900008 | en_US |
| dc.description | PubMed: 32073407 | en_US |
| dc.description.abstract | [Özet Yok] | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | LIPPINCOTT WILLIAMS & WILKINS | en_US |
| dc.relation.isversionof | 10.1097/MCD.0000000000000317 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | A novel mutation which causes a frameshift in thePHOX2Bgene causes Haddad syndrome | en_US |
| dc.type | article | en_US |
| dc.contributor.department | KKÜ | en_US |
| dc.identifier.volume | 29 | en_US |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.startpage | 152 | en_US |
| dc.identifier.endpage | 154 | en_US |
| dc.relation.journal | CLINICAL DYSMORPHOLOGY | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
