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. 105(3):640-657

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. 105(3):640-657