Robinow syndrome skeletal phenotypes caused by the WNT5AC83S variant are due to dominant interference with chondrogenesis.

Gignac SJ, Hosseini-Farahabadi S, Akazawa T, Schuck NJ, Fu K, Richman JM
Hum Mol Genet. 2019 Jul 15;28(14):2395-2414. doi: 10.1093/hmg/ddz071. PubMed Article

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