Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations

E.A. Colombo, H. Mutlu-Albayrak, Y. Shafeghati, M. Balasar, J. Piard, D. Gentilini, A.M. Di Blasio, C. Gervasini, L. Van Maldergem, L. Larizza

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