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Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects
Background: Craniosynostosis (CS) represents a highly heterogeneous genetic condition whose genetic background has not been yet revealed. The abnormality occurs either in isolated form or syndromic, as an element of hundreds of different inborn syndromes. Consequently, CS may often represent a chall...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112228/ https://www.ncbi.nlm.nih.gov/pubmed/35591945 http://dx.doi.org/10.3389/fmolb.2022.865494 |