학술논문
Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis
Document Type
Article
Author
Schrauwen, I.; Valgaeren, H.; Sommen, M.; Beyens, M.; Fransen, E.; Vandeweyer, G.; Schepers, A.; Van Camp, G.; Huentelman, M.J.; Tomas-Roca, L.; Rahmoun, M.; van Beusekom, E.; Gilissen, C.; Hoischen, A.; de Brouwer, A.P.M.; Kremer, H.; van Bokhoven, H.; Wesdorp, M.; Padberg, G.W.; Pennings, R.; Altunoglu, U.; De Leenheer, E.M.R.; Cremers, C.W.; Nasir, A.; Offeciers, E.; Dhooghe, I.; Huber, A.; Van de Heyning, P.; Zanetti, D.; Verbist, B.; Kayserili, H.
Source
In: Genetics in Medicine . (Genetics in Medicine, 1 May 2019, 21(5):1199-1208)
Subject
Language
English
ISSN
15300366
10983600
10983600