dc.contributor.author | Koruyucu, M. | |
dc.contributor.author | Gencay, K. | |
dc.contributor.author | HYUN, H-K | |
dc.contributor.author | LEE, Z. H. | |
dc.contributor.author | KIM, J-W | |
dc.contributor.author | Seymen, Figen | |
dc.contributor.author | Kasimoglu, Y. | |
dc.contributor.author | KIM, Y-J | |
dc.contributor.author | SHIN, T. J. | |
dc.date.accessioned | 2021-03-03T18:14:38Z | |
dc.date.available | 2021-03-03T18:14:38Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | KIM Y., Seymen F., Koruyucu M., Kasimoglu Y., Gencay K., SHIN T. J. , HYUN H., LEE Z. H. , KIM J., "Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta", ORAL DISEASES, cilt.22, sa.4, ss.297-302, 2016 | |
dc.identifier.issn | 1354-523X | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_4e01cd75-ddc1-4246-9e3d-fa5a86ef6fab | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/55735 | |
dc.identifier.uri | https://doi.org/10.1111/odi.12439 | |
dc.description.abstract | ObjectiveTo identify the molecular genetic aetiology of a family with autosomal dominant amelogenesis imperfecta (AI). | |
dc.language.iso | eng | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Diş Hekimliği | |
dc.subject | Sağlık Bilimleri | |
dc.subject | DİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP | |
dc.subject | Klinik Tıp | |
dc.title | Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta | |
dc.type | Makale | |
dc.relation.journal | ORAL DISEASES | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 22 | |
dc.identifier.issue | 4 | |
dc.identifier.startpage | 297 | |
dc.identifier.endpage | 302 | |
dc.contributor.firstauthorID | 102845 | |