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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
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 |