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Crouzon Syndrome: a Comprehensive Review
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying pathological process is premature synostosis of the cranial sutures with subsequent phenotypic alterations of the affected person. A review of the literature has been conducted in order to resume the over...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Balkan Stomatological Society
2018-03-01
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| Colecção: | Balkan Journal of Dental Medicine |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.2478/bjdm-2018-0001 |
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