Commentary on "Craniofacial Syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis"

Pediatr Res. 2024 May;95(6):1412-1414. doi: 10.1038/s41390-024-03036-3. Epub 2024 Jan 20.
No abstract available

MeSH terms

  • Craniofacial Abnormalities / genetics
  • Genotype*
  • Humans
  • Phenotype*
  • Syndrome