Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome
| dc.contributor.author | Özlü, Emin | |
| dc.contributor.author | Karadağ, Ayşe Serap | |
| dc.contributor.author | Akalın, İbrahim | |
| dc.contributor.author | Yeşil, Gözde | |
| dc.contributor.author | Yılmaz, Sarenur | |
| dc.contributor.author | Zindancı, İlkin | |
| dc.contributor.author | Akdeniz, Necmettin | |
| dc.date.accessioned | 2020-04-30T23:19:44Z | |
| dc.date.available | 2020-04-30T23:19:44Z | |
| dc.date.issued | 2019 | |
| dc.department | DÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
| dc.description | WOS: 000524236100005 | en_US |
| dc.description.abstract | … | en_US |
| dc.identifier.doi | 10.5021/ad.2019.31.S.S10 | en_US |
| dc.identifier.endpage | S11 | en_US |
| dc.identifier.issn | 1013-9087 | |
| dc.identifier.issn | 2005-3894 | |
| dc.identifier.startpage | S10 | en_US |
| dc.identifier.uri | https://doi.org/10.5021/ad.2019.31.S.S10 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12684/3839 | |
| dc.identifier.volume | 31 | en_US |
| dc.identifier.wos | WOS:000524236100005 | en_US |
| dc.identifier.wosquality | Q3 | en_US |
| dc.indekslendigikaynak | Web of Science | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Korean Dermatological Assoc | en_US |
| dc.relation.ispartof | Annals Of Dermatology | en_US |
| dc.relation.publicationcategory | Diğer | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome | en_US |
| dc.type | Editorial | en_US |
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