A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome
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Title
A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 26, Issue 7, Pages 1280-1293
Publisher
Oxford University Press (OUP)
Online
2017-02-07
DOI
10.1093/hmg/ddx029
References
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- (2011) T. Kizhner et al. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
- New insights into the molecular mechanism of multiple synostoses syndrome (SYNS): Mutation within the GDF5 knuckle epitope causes noggin-resistance
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- (2010) Peter Dy et al. DEVELOPMENTAL BIOLOGY
- Fgf-9 is required for angiogenesis and osteogenesis in long bone repair
- (2010) B. Behr et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- 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
- FGF9 monomer–dimer equilibrium regulates extracellular matrix affinity and tissue diffusion
- (2009) Masayo Harada et al. NATURE GENETICS
- A critical evaluation of specific aspects of joint development
- (2008) A.A. Pitsillides et al. DEVELOPMENTAL DYNAMICS
- High-resolution in situ hybridization to whole-mount zebrafish embryos
- (2007) Christine Thisse et al. Nature Protocols
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