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Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations

TCF12 mutations have been reported very recently in coronal synostosis. We report several cases of familial coronal synostosis among four families harbouring novel TCF12 mutations. We observed a broad interfamilial phenotypic spectrum with features overlapping with the Saethre–Chotzen syndrome. TCF1...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: di Rocco, Federico, Baujat, Geneviève, Arnaud, Eric, Rénier, Dominique, Laplanche, Jean-Louis, Daire, Valérie Cormier, Collet, Corinne
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4231413/
https://ncbi.nlm.nih.gov/pubmed/24736737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.57
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