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Diffusion Tensor Imaging and Fiber Tractography in Children with Craniosynostosis Syndromes
BACKGROUND AND PURPOSE: Patients with craniosynostosis syndromes caused by mutations in FGFR-2, FGFR-3, and TWIST1 genes are characterized by having prematurely fused skull sutures and skull base synchondroses, which result in a skull deformity and are accompanied by brain anomalies, including alter...
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| Pubblicato in: | AJNR Am J Neuroradiol |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society of Neuroradiology
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7964691/ https://ncbi.nlm.nih.gov/pubmed/25953762 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A4301 |
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