PedAM
Pediatric Disease Annotations & Medicines
| Disease | craniosynostosis |
| Phenotype | C0175699|saethre-chotzen syndrome |
| Sentences | 1 |
| PubMedID- 23738319 | In addition to the fgfr signaling mutations, twist1 is implicated in craniosynostosis in humans with saethre-chotzen syndrome [33–36]. |
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