Persistent URL of this record https://hdl.handle.net/1887/121901
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Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis
- All authors
- Schrauwen, I.; Valgaeren, H.; Tomas-Roca, L.; Sommen, M.; Altunoglu, U.; Wesdorp, M.; Beyens, M.; Fransen, E.; Nasir, A.; Vandeweyer, G.; Schepers, A.; Rahmoun, M.; Beusekom, E. van; Huentelman, M.J.; Offeciers, E.; Dhooghe, I.; Huber, A.; Heyning, P. van de; Zanetti, D.; Leenheer, E.M.R. de; Gilissen, C.; Hoischen, A.; Cremers, C.W.; Verbist, B.; Brouwer, A.P.M. de; Padberg, G.W.; Pennings, R.; Kayserili, H.; Kremer, H.; Camp, G. van; Bokhoven, H. van
- Date
- 2019-05-01
- Journal
- Genetics in Medicine
- Volume
- 21
- Issue
- 5
- Pages
- 1199 - 1208