Reactome | Reardon, W

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created	[InstanceEdit:2023281] Rothfels, K, 2011-12-07
dbId	2023282
displayName	Reardon, W
firstname	William
initial	W
publications	[LiteratureReference:2060840] Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis [LiteratureReference:2023308] A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome [LiteratureReference:2029815] Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome
schemaClass	Person
surname	Reardon

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