dc.contributor.author | Huentelman, M. J. | |
dc.contributor.author | Valgaeren, H. | |
dc.contributor.author | Schrauwen, I. | |
dc.contributor.author | Tomas-Roca, L. | |
dc.contributor.author | Wesdorp, M. | |
dc.contributor.author | Sommen, M. | |
dc.contributor.author | Rahmouni, M. | |
dc.contributor.author | van Beusekom, E. | |
dc.contributor.author | Offeciers, E. | |
dc.contributor.author | dHooghe, I. | |
dc.contributor.author | Vincent, R. | |
dc.contributor.author | Huber, A. | |
dc.contributor.author | Van de Heyning, P. | |
dc.contributor.author | Zanetti, D. | |
dc.contributor.author | De Leenheer, E. M. R. | |
dc.contributor.author | Gilissen, C. | |
dc.contributor.author | Cremers, C. W. | |
dc.contributor.author | Verbist, B. | |
dc.contributor.author | de Brouwer, A. P. M. | |
dc.contributor.author | Padberg, G. W. | |
dc.contributor.author | Kremer, H. | |
dc.contributor.author | Van Camp, G. | |
dc.contributor.author | van Bokhoven, H. | |
dc.contributor.author | Altunoglu, U. | |
dc.date.accessioned | 2021-03-02T22:51:09Z | |
dc.date.available | 2021-03-02T22:51:09Z | |
dc.identifier.citation | Valgaeren H., Schrauwen I., Tomas-Roca L., Altunoglu U., Wesdorp M., Sommen M., Rahmouni M., van Beusekom E., Huentelman M. J. , Offeciers E., et al., "Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis", 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.67-68 | |
dc.identifier.other | av_0f17440f-4c99-4d36-ab01-4732aee11254 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/15673 | |
dc.language.iso | eng | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Temel Bilimler | |
dc.subject | Sitogenetik | |
dc.subject | BİYOKİMYA VE MOLEKÜLER BİYOLOJİ | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | GENETİK VE HAYAT | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıbbi Genetik | |
dc.title | Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis | |
dc.type | Bildiri | |
dc.contributor.department | University of Antwerp , , | |
dc.identifier.volume | 26 | |
dc.contributor.firstauthorID | 154906 | |