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Ciliary Signalling and Mechanotransduction in the Pathophysiology of Craniosynostosis
Craniosynostosis (CS) is the second most prevalent inborn craniofacial malformation; it results from the premature fusion of cranial sutures and leads to dimorphisms of variable severity. CS is clinically heterogeneous, as it can be either a sporadic isolated defect, more frequently, or part of a sy...
Bewaard in:
| Gepubliceerd in: | Genes (Basel) |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
MDPI
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8306115/ https://ncbi.nlm.nih.gov/pubmed/34356089 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12071073 |
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