Persistent URL of this record https://hdl.handle.net/1887/3195923
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SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling
- All authors
- Lin, Y.C.; Niceta, M.; Muto, V.; Vona, B.; Pagnamenta, A.T.; Maroofian, R.; Beetz, C.; Duyvenvoorde, H. van; Dentici, M.L.; Lauffer, P.; Vallian, S.; Ciolfi, A.; Pizzi, S.; Bauer, P.; Gruning, N.M.; Bellacchio, E.; Fattore, A. del; Petrini, S.; Shaheen, R.; Tiosano, D.; Halloun, R.; Pode-Shakked ben; Albayrak, H.M.; Isik, E.; Wit, J.M.; Dittrich, M.; Freire, B.L.; Bertola, D.R.; Jorge, A.A.L.; Barel, O.; Sabir, A.H.; Tenaiji, A.M.J. al; Taji, S.M.; Al-Sannaa, N.; Al-Abdulwahed, H.; Digilio, M.C.; Irving, M.; Anikster, Y.; Bhavani, G.S.L.; Girisha, K.M.; Haaf, T.; Taylor, J.C.; Dallapiccola, B.; Alkuraya, F.S.; Yang, R.B.; Tartaglia, M.; Genomics England Res Consortium
- Date
- 2021-01-07
- Volume
- 108
- Issue
- 1
- Pages
- 115 - 133