- Intraosseous atypical chondroid tumor or chondrosarcoma grade 1 in patients with multiple osteochondromas(2015)
Authors: Annemarie L. Goud, Wim Wuyts, Johannes Bessems, Jos Bramer, Henk Jan van der Woude, John Ham
Pages: 24 - 31
- DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies(2015)
Authors: Maja Sukalo, Felix Tilsen, Huelya Kayserili, Dietmar Mueller, Beyhan Tueysuez, Deborah M. Ruddy, Emma Wakeling, Karen Helene Orstavik, Katie M. Snape, Richard Trembath, et al.
Pages: 593 - 598
- Isolated terminal limb reduction defects(2014)
Authors: Mala Isrie, Wim Wuyts, Hilde Van Esch, Koenraad Devriendt
Pages: 1576 - 1579
- EMQN best practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus(2013)
Authors: Lies H. Hoefsloot, Anne-Françoise Roux, Maria Bitner-Glindzicz, Wim Wuyts
Pages: 1325 - 1329
- tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans(2013)
Authors: Mariana Igoillo-Esteve, Anne Genin, Nelle Lambert, Wim Wuyts, et al.
Pages: 1 - 15
- Hereditary multiple osteochondromas(2013)
Authors: Wim Wuyts, G.A. Schmale, H.A. Chansky, W.H. Raskind
- A new double substitution mutation in the MEN1 gene(2013)
Authors: Urielle Ullmann, David Unuane, Brigitte Velkeniers, Willy Lissens, Wim Wuyts, Maryse Bonduelle
Pages: 695 - 697
- Identification and functional characterization of the human **EXT1** promoter region(2012)
Authors: Ivy Jennes, Monia Zuntini, Kirsten Mees, Ajay Palagani, Elena Pedrini, Greet De Cock, Erik Fransen, Wim Vanden Berghe, Luca Sangiorgi, Wim Wuyts
Pages: 148 - 159
- Tiling resolution array-CGH shows that somatic mosaic deletion of the **EXT** gene is causative in **EXT** gene mutation negative multiple osteochondromas patients(2011)
Authors: Károly Szuhai, Ivy Jennes, Danielle de Jong, Judith V.M.G. Bovée, Malgorzata Wiweger, Wim Wuyts, Pancras C.W. Hogendoorn
Pages: E2036 - E2049
- Clinical and molecular studies of EXT1/EXT2 in Bulgaria(2011)
Authors: Malina Kirilova Stancheva-Ivanova, Wim Wuyts, Els van Hul, Briguita Ivanova Radeva, Radoslava Vasileva Vazharova, Todor Petrov Sokolov, Borislav Yordanov Vladimirov, Margarita Dimitrova Apostolova, Ivo Marinov Kremensky
Pages: 917 - 921
