FBXO11

Publications

Jansen S et al. De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioural problems and dysmorphisms. Eur J Hum Genet. 2019;27(5):738-746 PMID: 30679813.

Gregor et al. De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. Am J Hum Genet. 2018;103(2):305-316. PMID: 30057029.

Martinez F et al. High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing. J Med Genet. 2017;54(2):87-92. PMID: 27620904.