FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family
Published 2023 View Full Article
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Title
FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family
Authors
Keywords
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Journal
Genes
Volume 14, Issue 3, Pages 724
Publisher
MDPI AG
Online
2023-03-16
DOI
10.3390/genes14030724
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Related references
Note: Only part of the references are listed.- Novel FGF9 variant contributes to multiple synostoses syndrome 3
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- Fgf9 Negatively Regulates Bone Mass by Inhibiting Osteogenesis and Promoting Osteoclastogenesis Via MAPK and PI3K / AKT Signaling
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- Wide spectrum of congenital anomalies including choanal atresia, malformed extremities, and brain and spinal malformations in a girl with a de novo 5.6-Mb deletion of 13q12.11-13q12.13
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- FGF9 monomer–dimer equilibrium regulates extracellular matrix affinity and tissue diffusion
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