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1 ensaios clínicos encontrados.
FGFR1:TACC1-Fused Pilocytic Astrocytoma in a Child With Muenke Syndrome: A Case Report.
Isolated frontosphenoidal craniosynostosis with pathogenic FGFR3 variant: a case report and genetic insights.
Semi-automated three-dimensional analysis of maxillary anomalies in patients with Muenke syndrome, Saethre-Chotzen syndrome or TCF12-related craniosynostosis: A retrospective study.
Reversible abducens nerve palsy following cranial vault expansion in the setting of multisutural craniosynostosis: illustrative case.
[A case report of Muenke syndrome with soft cleft palate and literature review].