Associated Papers
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.
Tønne E et al.
European Journal of Human Genetics : Ejhg, 2021
Coronal craniosynostosis due to TCF12 mutations in patients from Turkey.
Yilmaz E et al.
American Journal of Medical Genetics. Part A, 2019
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
Sharma VP et al.
Nature Genetics, 2013
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