Craniofacial abnormalities in a murine model of Saethre-Chotzen Syndrome.

CONCLUSIONS: The skeletal and dental alterations in the height, length and width provide a foundation for large-scale phenomics studies, which will improve existing knowledge of the Twist1 signalling cascade. This is relevant given the predicted shift in minimally invasive molecular medical treatment for craniosynostosis. PMID: 31199981 [PubMed - as supplied by publisher]
Source: Annals of Anatomy - Category: Anatomy Authors: Tags: Ann Anat Source Type: research
More News: Anatomy | Genetics | Study