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Select item 100483041.

FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family

Ariane Schmetz, Jörg Schaper, Simon Thelen, Majeed Rana, Thomas Klenzner, Katharina Schaumann, Jasmin Beygo, Harald Surowy, Hermann-Josef Lüdecke, Dagmar Wieczorek

Genes (Basel) 2023 Mar; 14(3): 724. Published online 2023 Mar 15. doi: 10.3390/genes14030724

PMCID:: PMC10048304

Article PDF–8.5M

Select item 78394472.

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

Ann‐Charlotte Thuresson, Brittany Croft, Yasmin D. Hailer, Gunnar Liminga, Carl‐Göran Arvidsson, Vincent R. Harley, Eva‐Lena Stattin

Clin Genet. 2021 Feb; 99(2): 325–329. Published online 2021 Jan 13. doi: 10.1111/cge.13880

PMCID:: PMC7839447

Article PDF–2.0M

Select item 27069693.

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

Xiao-lin Wu, Ming-min Gu, Lei Huang, Xue-song Liu, Hong-xin Zhang, Xiao-yi Ding, Jian-qiang Xu, Bin Cui, Long Wang, Shun-yuan Lu, Xiao-yi Chen, Hai-guo Zhang, Wei Huang, Wen-tao Yuan, Jiang-ming Yang, Qun Gu, Jian Fei, Zhu Chen, Zhi-min Yuan, Zhu-gang Wang

Am J Hum Genet. 2009 Jul 10; 85(1): 53–63. doi: 10.1016/j.ajhg.2009.06.007