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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
Nat Genet. 2013 Mar;45(3):304-7. doi: 10.1038/ng.2531. Epub 2013 Jan 27.
Nat Genet. 2013.
PMID: 23354436
Free PMC article.
Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome.
Teng CS, Ting MC, Farmer DT, Brockop M, Maxson RE, Crump JG.
Teng CS, et al.
Elife. 2018 Oct 25;7:e37024. doi: 10.7554/eLife.37024.
Elife. 2018.
PMID: 30375332
Free PMC article.
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