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Genetic advances in craniosynostosis
Craniosynostosis, the premature ossification of one or more skull sutures, is a clinically and genetically heterogeneous congenital anomaly affecting approximately 1 in 2,500 live births. In most cases, it occurs as an isolated congenital anomaly, i.e. nonsyndromic craniosynostosis (NCS), the geneti...
Gardado en:
| Publicado en: | Am J Med Genet A |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5397362/ https://ncbi.nlm.nih.gov/pubmed/28160402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38159 |
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