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Genetic mutations in Gorlin-Goltz syndrome
Gorlin-Goltz syndrome is a rare multisystemic disease inherited in a dominant autosomal at a high level of penetrance and variable expressiveness. It is mainly characterized by basal cell carcinoma, odontogenic keratocyst and skeletal anomalies. Diagnosis is based upon established major and minor cl...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3841570/ https://ncbi.nlm.nih.gov/pubmed/24339558 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.120810 |
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