Gorlin-Goltz syndrome: A rare case report
Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts (OKCs) and musculoskeletal malformations. A rare case of this syndrome observed in a 13-year-old male patient is presented in which multiple OKCs were c...
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| Materiálatiipa: | Girji |
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Wolters Kluwer Medknow Publications,
2013-01-01T00:00:00Z.
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