A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3

Ovotesticular disorders of sex development (DSD) in FGF9 mouse models of human synostosis syndromes

(2020) Anthony D Bird et al.   HUMAN MOLECULAR GENETICS

A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome

(2017) Lingyun Tang et al.   HUMAN MOLECULAR GENETICS

FGF9 mutation causes craniosynostosis along with multiple synostoses

(2017) Maria Rodriguez-Zabala et al.   HUMAN MUTATION

Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization

(2017) Yang Liu et al.   STRUCTURE

Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

(2009) Xiao-lin Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Homodimerization Controls the Fibroblast Growth Factor 9 Subfamily's Receptor Binding and Heparan Sulfate-Dependent Diffusion in the Extracellular Matrix

(2009) J. Kalinina et al.   MOLECULAR AND CELLULAR BIOLOGY

FGF9 monomer–dimer equilibrium regulates extracellular matrix affinity and tissue diffusion

(2009) Masayo Harada et al.   NATURE GENETICS