Holt, Richard J ;
Young, Rodrigo M ;
Crespo, Berta...
Holt , R J , Young , R M , Crespo , B , Ceroni , F , Curry , C J , Bellacchio , E , Bax , D A , Ciolfi , A , Simon , M , Fagerberg , C R , van Binsbergen , E , De Luca , A , Memo , L , Dobyns , W B , Mohammed , A A , Clokie , S J H , Zazo Seco , C , Jiang , Y H , Sørensen , K P , Andersen , H , Sullivan , J , Powis , Z , Chassevent , A , Smith-Hicks , C , Petrovski , S , Antoniadi , T , Shashi , V , Gelb , B D , Wilson , S W , Gerrelli , D , Tartaglia , M , Chassaing , N , Calvas , P & Ragge , N K 2019 , ' De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies ' , American Journal of Human Genetics , vol. 105 , no. 3 , pp. 640-657 . https://doi.org/10.1016/j.ajhg.2019.07.005.
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2019
