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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
- Published in:
- Nature Genetics, 2013, v. 45, n. 10, p. 1261, doi. 10.1038/ng1013-1261a
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- Article
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
- Published in:
- Nature Genetics, 2013, v. 45, n. 3, p. 304, doi. 10.1038/ng.2531
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- Publication type:
- Article
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
- Published in:
- Human Genetics, 2020, v. 139, n. 8, p. 1077, doi. 10.1007/s00439-020-02157-z
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- Publication type:
- Article