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
Identification of the third FGF9 variant in a girl with multiple synostosis-comparison of the genotype:phenotype of FGF9 variants in humans and mice.
Sentchordi-Montané L et al.
Clinical Genetics, 2021
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