Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene()

Studies in mice demonstrated that the Shh gene is crucial for normal development of both incisors and molars, causing a severe retardation in tooth growth, which leads to abnormal placement of the tooth in the jaw and disrupted tooth morphogenesis. In humans the SHH gene is located on chromosome 7q3...

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Detalles Bibliográficos
Autores principales: Linhares, Natália D., Svartman, Marta, Salgado, Mauro Ivan, Rodrigues, Tatiane C., da Costa, Silvia S., Rosenberg, Carla, Valadares, Eugênia R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287791/
https://www.ncbi.nlm.nih.gov/pubmed/25606385
http://dx.doi.org/10.1016/j.mgene.2013.10.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287791/
https://www.ncbi.nlm.nih.gov/pubmed/25606385
http://dx.doi.org/10.1016/j.mgene.2013.10.005

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