De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.
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Holt RJ, et al. Among authors: wilson sw.
Am J Hum Genet. 2019 Sep 5;105(3):640-657. doi: 10.1016/j.ajhg.2019.07.005. Epub 2019 Aug 8.
Am J Hum Genet. 2019.
PMID: 31402090
Free PMC article.