Clinical spectrum of fibroblast growth factor receptor mutations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference106 articles.
1. Achondroplasia in Sweden caused by the G1 138A mutation in FGFR3
2. Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand
3. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
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