Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations
暂无分享,去创建一个
E. Colombo | D. Gentilini | L. Larizza | L. Van Maldergem | C. Gervasini | Y. Shafeghati | J. Piard | A. D. Di Blasio | Hatice Mutlu-Albayrak | Mine Balasar