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Dental and Craniofacial Anomalies Associated with Axenfeld-Rieger Syndrome with PITX2 Mutation
Axenfeld-Rieger syndrome (ARS) (OMIM Nr.: 180500) is a rare autosomal dominant disorder (1 : 200000) with genetic and morphologic variability. Glaucoma is associated in 50% of the patients. Craniofacial and dental anomalies are frequently reported with ARS. The present study was designed as a mult...
Autores principales: | Dressler, Simone, Meyer-Marcotty, Philipp, Weisschuh, Nicole, Jablonski-Momeni, Anahita, Pieper, Klaus, Gramer, Gwendolyn, Gramer, Eugen |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2842968/ https://www.ncbi.nlm.nih.gov/pubmed/20339518 http://dx.doi.org/10.1155/2010/621984 |
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