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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CASE REPORT
Published on 15 Sep 2025
ORIGINAL RESEARCH
Published on 31 Jul 2025
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