Search Results - "Swinnen, Steven"

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis by Ockeloen, Charlotte W., Khandelwal, Kriti D., Dreesen, Karoline, Ludwig, Kerstin U., Sullivan, Robert, van Rooij, Iris A.L.M., Thonissen, Michelle, Swinnen, Steven, Phan, Milien, Conte, Federica, Ishorst, Nina, Gilissen, Christian, Roa Fuentes, Laury, van de Vorst, Maartje, Henkes, Arjen, Steehouwer, Marloes, van Beusekom, Ellen, Bloemen, Marjon, Vankeirsbilck, Bruno, Bergé, Stefaan, Hens, Greet, Schoenaers, Joseph, Vander Poorten, Vincent, Roosenboom, Jasmien, Verdonck, An, Devriendt, Koen, Roeleveldt, Nel, Jhangiani, Shalini N., Vissers, Lisenka E.L.M., Lupski, James R., de Ligt, Joep, Von den Hoff, Johannes W., Pfundt, Rolph, Brunner, Han G., Zhou, Huiqing, Dixon, Jill, Mangold, Elisabeth, van Bokhoven, Hans, Dixon, Michael J., Kleefstra, Tjitske, Hoischen, Alexander, Carels, Carine E.L.

“…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…”
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Tooth agenesis patterns and phenotype variation in a cohort of Belgian patients with hypodontia and oligodontia clustered in 79 families with their pedigrees by Dreesen, Karoline, Swinnen, Steven, Devriendt, Koenraad, Carels, Carine

“…Even though tooth agenesis is the most common developmental anomaly of the human dentition, its genetic background and pathogenic mechanism(s) still remain…”
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The effect of using CBCT in the diagnosis of canine impaction and its impact on the orthodontic treatment outcome by Alqerban, Ali, Jacobs, Reinhilde, van Keirsbilck, Pieter-Jan, Aly, Medhat, Swinnen, Steven, Fieuws, Steffen, Willems, Guy

“…Aim: To investigate the added-value of using CBCT in the orthodontic treatment method of maxillary impacted canines and treatment outcome. Materials and…”
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Orthodontic and orthognathic management of a patient with Apert syndrome: a case report by Verdonck, Anna, Bertrand, Julie, Carels, Carine, Swinnen, Steven, Schoenaers, Joseph

“…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…”
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