Associated Papers
A novel FBXW11 variant in a patient with neurodevelopmental, jaw, eye, and digital syndrome.
Maznina A et al.
Neurogenetics, 2025
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.
Holt RJ et al.
American Journal of Human Genetics, 2019
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