Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes

Craniosynostosis is a birth defect where calvarial sutures close prematurely, as part of a genetic syndrome or independently, with unknown cause. This study aimed to identify differences in gene expression in primary calvarial cell lines derived from patients with four phenotypes of single-suture cr...

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Detalles Bibliográficos
Autores principales: Lapehn, Samantha, Gustafson, Jonas A., Timms, Andrew E., Cunningham, Michael L., Paquette, Alison G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049207/
https://www.ncbi.nlm.nih.gov/pubmed/36982425
http://dx.doi.org/10.3390/ijms24065353

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049207/
https://www.ncbi.nlm.nih.gov/pubmed/36982425
http://dx.doi.org/10.3390/ijms24065353

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