Associated Papers
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis.
Luyckx I et al.
Journal of Medical Genetics, 2024
Clinical interest of molecular study in cases of isolated midline craniosynostosis.
Di Rocco F et al.
European Journal of Human Genetics : Ejhg, 2023
Impact of SMAD6 Variants on Neurodevelopment in Craniosynostosis.
Verlut I et al.
The Journal of Craniofacial Surgery, 0
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