FGFs, their receptors, and human limb malformations: Clinical and molecular correlations
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference89 articles.
1. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
2. Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand
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4. Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype
5. An Intronic Sequence Element Mediates Both Activation and Repression of Rat Fibroblast Growth Factor Receptor 2 Pre-mRNA Splicing
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