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Discussion of "Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?"

The Journal of craniofacial surgery - 1 May 2023

Raposo-Amaral Cassio Eduardo, Raposo-Amaral Cesar Augusto, Ghizoni Enrico

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PMID: 36727961
DOI: 10.1097/SCS.0000000000009173

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Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?Semantic proximity Read ↗

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FGFR2 gene Related Apert and Crouzon Syndrome Patients with Different Craniofacial Dysmorphisms: A Systematic Review and Meta-analysisSemantic proximity Read ↗

European Guideline Robin Sequence An Initiative From the European Reference Network for Rare Craniofacial Anomalies and Ear, Nose and Throat Disorders (ERN-CRANIO)Semantic proximity Read ↗

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