Gorlin-Goltz syndrome

Gorlin-Goltz syndrome is an inherited autosomal dominant disorder with complete penetrance and extreme variable expressivity. The authors present a case of an 11-year-old girl with typical features of Gorlin-Goltz syndrome with special respect to medical and dental problems which include multiple bo...

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Detalles Bibliográficos
Autores principales: Kohli, Munish, Kohli, Monica, Sharma, Naresh, Siddiqui, Saif Rauf, Tulsi, S.P.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304191/
https://www.ncbi.nlm.nih.gov/pubmed/22442551
http://dx.doi.org/10.4103/0975-5950.69171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304191/
https://www.ncbi.nlm.nih.gov/pubmed/22442551
http://dx.doi.org/10.4103/0975-5950.69171

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