Associated Papers
FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family.
Schmetz A et al.
Genes, 2023
FGF9 variant in 46,XY DSD patient suggests a role for dimerization in sex determination.
Croft B et al.
Clinical Genetics, 2023
Novel FGF9 variant contributes to multiple synostoses syndrome 3.
Dobson SM et al.
American Journal of Medical Genetics. Part A, 2022
A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3.
Thuresson AC et al.
Clinical Genetics, 2021
Cervical vertebrae fusion in elbow knee synostosis (Eks)-mutant mice with fibroblast growth factor 9 N143T mutation.
Djameh G et al.
Congenital Anomalies, 0
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