CASE REPORT
Published on 15 Sep 2025
A Chinese premature infant with cleidocranial dysplasia characterized by heterozygous RUNX2 mutation and cerebral infarction: a case report
doi 10.3389/fped.2025.1643266
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- Frontiers in Dental Medicine
- Systems Integration
- Research Topics
- Innovative Approaches in Craniofacial Defect Reconstruction: Bridging Clinical and Basic Science
Innovative Approaches in Craniofacial Defect Reconstruction: Bridging Clinical and Basic Science
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