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GORLIN'S SYNDROME: CASE REPORT AND MANAGEMENT PROTOCOL

dc.contributor.authorKayserili, H.
dc.contributor.authorYalcin, S.
dc.contributor.authorAktas, I
dc.contributor.authorRosti, R. O.
dc.date.accessioned2021-03-02T21:30:51Z
dc.date.available2021-03-02T21:30:51Z
dc.date.issued2009
dc.identifier.citationRosti R. O. , Aktas I., Kayserili H., Yalcin S., "GORLIN'S SYNDROME: CASE REPORT AND MANAGEMENT PROTOCOL", BALKAN JOURNAL OF MEDICAL GENETICS, cilt.12, sa.1, ss.61-65, 2009
dc.identifier.issn1311-0160
dc.identifier.othervv_1032021
dc.identifier.otherav_076869b3-fb6c-450d-bfb3-6837e00813d6
dc.identifier.urihttp://hdl.handle.net/20.500.12627/10812
dc.identifier.urihttps://doi.org/10.2478/v10034-009-0002-z
dc.description.abstractGorlin's syndrome (GS) is a rare autosomal, dominant syndrome, characterized by multiple basal cell carcinomas, odontogenic keratocysts, a characteristic facial appearance, skeletal anomalies and malignancies of various organs throughout the body. We describe a 14-year-old girl with GS and propose a management protocol.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleGORLIN'S SYNDROME: CASE REPORT AND MANAGEMENT PROTOCOL
dc.typeMakale
dc.relation.journalBALKAN JOURNAL OF MEDICAL GENETICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume12
dc.identifier.issue1
dc.identifier.startpage61
dc.identifier.endpage65
dc.contributor.firstauthorID190484


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