Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Steven Swinnen"'
Autor:
Michelle Thonissen, Marloes Steehouwer, Maartje van de Vorst, K Dreesen, Shalini N. Jhangiani, Carine Carels, Han G. Brunner, Marjon Bloemen, Vincent Vander Poorten, Joep de Ligt, Elisabeth Mangold, Christian Gilissen, Charlotte W. Ockeloen, Joseph Schoenaers, Ellen van Beusekom, Nina Ishorst, Federica Conte, Rolph Pfundt, Tjitske Kleefstra, Robert Sullivan, Huiqing Zhou, Lisenka E.L.M. Vissers, Anna Verdonck, Iris A.L.M. van Rooij, Johannes W. Von den Hoff, Kriti D. Khandelwal, Arjen Henkes, Koenraad Devriendt, Alexander Hoischen, Bruno Vankeirsbilck, Milien Phan, Nel Roeleveldt, Greet Hens, James R. Lupski, Jasmien Roosenboom, Steven Swinnen, Stefaan J. Bergé, Hans van Bokhoven, Kerstin U. Ludwig, Laury A Roa Fuentes, Michael J. Dixon, Jill Dixon
Publikováno v:
Genetics in Medicine, 18, 11, pp. 1158-1162
Genetics in Medicine, 18(11), 1158. Lippincott Williams and Wilkins
Genetics in medicine : official journal of the American College of Medical Genetics
Genetics in Medicine, 18, 1158-1162
Genetics in Medicine, 18(11), 1158. Lippincott Williams and Wilkins
Genetics in medicine : official journal of the American College of Medical Genetics
Genetics in Medicine, 18, 1158-1162
Contains fulltext : 165724.pdf (Publisher’s version ) (Open Access) PURPOSE: We aimed to identify a novel genetic cause of tooth agenesis (TA) and/or orofacial clefting (OFC) by combining whole-exome sequencing (WES) and targeted resequencing in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e2c78055fa8f0e3492994b5a4e48e8
https://hdl.handle.net/2066/165724
https://hdl.handle.net/2066/165724
Autor:
Steven Swinnen, Guy Willems, Pieter‑Jan van Keirsbilck, Steffen Fieuws, Ali Alqerban, Medhat Aly, Reinhilde Jacobs
Publikováno v:
Journal of Orthodontic Science
Aim: To investigate the added‑value of using CBCT in the orthodontic treatment method of maxillary impacted canines and treatment outcome. Materials and Methods: The sample consisted of 118 treated patients. The CBCT group (n = 58) (39 females/19 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3442e372b6bb84c1154da7cc7e146e08
http://www.jorthodsci.org/article.asp?issn=2278-0203
http://www.jorthodsci.org/article.asp?issn=2278-0203
Publikováno v:
European Journal of Orthodontics, 36, 99-106
European Journal of Orthodontics, 36, 1, pp. 99-106
European Journal of Orthodontics, 36, 1, pp. 99-106
BACKGROUND: Even though tooth agenesis is the most common developmental anomaly of the human dentition, its genetic background and pathogenic mechanism(s) still remain poorly understood. Syndromic and isolated forms of hypodontia have been described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d2505cfd04b176b8362e91b30ffdcf3
https://doi.org/10.1093/ejo/cjt021
https://doi.org/10.1093/ejo/cjt021
Publikováno v:
Journal of Orthodontics, 37, 2, pp. 121-7
Journal of Orthodontics, 37, 121-7
Journal of Orthodontics, 37, 121-7
Item does not contain fulltext This case report describes the combined orthodontic and orthognathic management of a 14-year-old girl affected with Apert syndrome. She presented with a severe Class III skeletal relationship, midfacial hypoplasia and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae29464b90bac709ff28a7a7a8e3a4a2
https://hdl.handle.net/2066/89890
https://hdl.handle.net/2066/89890