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Common primary fibroblastic growth factor receptor-related craniosynostosis syndromes: A pictorial review
Mutations in different types of fibroblastic growth factor receptors (FGFRs) have been associated with a variety of phenotype abnormalities, the common ones being Apert, Crouzon and Pfeiffer syndromes. In this study, we present two representative cases having the Apert and Pfeiffer syndromes, respec...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964784/ https://www.ncbi.nlm.nih.gov/pubmed/21042516 http://dx.doi.org/10.4103/1817-1745.66685 |