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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Detalles Bibliográficos
Autores principales: Daneswari, Muthumula, Reddy, Mutjumula Swamy Ranga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841570/
https://www.ncbi.nlm.nih.gov/pubmed/24339558
http://dx.doi.org/10.4103/0971-6866.120810

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841570/
https://www.ncbi.nlm.nih.gov/pubmed/24339558
http://dx.doi.org/10.4103/0971-6866.120810

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