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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

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