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De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

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Description scientific article published on 08 August 2019
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author: Samuel J Clokie  Christina Fagerberg  William B. Dobyns  Rodrigo M Young  Alessandro De Luca  Stephen W Wilson  Dianne Gerrelli 

Publication date August 8, 2019
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