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Clinicopathologic and Molecular Characteristics of Familial Cherubism with Associated Odontogenic Tumorous Proliferations

Cherubism is a rare autosomal dominant condition affecting the jaws and caused by mutations in the gene encoding for the adapter protein SH3BP2 that maps to chromosome 4p16.3. Cherubism is characterized by symmetrically developing bone lesions in the maxilla and mandible. The lesions have been radio...

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Bibliografische gegevens
Gepubliceerd in:Head Neck Pathol
Hoofdauteurs: Argyris, Prokopios P., Gopalakrishnan, Rajaram, Hu, Ying, Reichenberger, Ernst J., Koutlas, Ioannis G.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Springer US 2017
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5873491/
https://ncbi.nlm.nih.gov/pubmed/28721660
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12105-017-0837-7
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