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Displaying 2 results.

- Journal article
Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
Kelley, Brian P. Malfait, Fransiska Bonafe, Luisa Baldridge, Dustin Homan, Erica Symoens, Sofie Willaert, Andy Elcioglu, Nursel Van Maldergem, Lionel Verellen-Dumoulin, Christine[UCL] Gillerot, Yves[UCL] Napierala, Dobrawa Krakow, Deborah Beighton, Peter Superti-Furga, Andrea De Paepe, Anne Lee, Brendan (2011) Journal of Bone and Mineral Research — Vol. 26, no. 3, p. 666-672 (2011)
- Journal article
Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers.
Lantoine, Joséphine Brysse, Anne Dideberg, Vinciane Claes, Kathleen Symoens, Sofie Coucke, Wim Benoit, Valérie Rombout, Sonia De Rycke, Martine Seneca, Sara Van Laer, Lut Wuyts, Wim Corveleyn, Anniek Van Den Bogaert, Kris Rydlewski, Catherine Wilkin, Françoise Ravoet, Marie[UCL] Fastré, Elodie[UCL] Capron, Arnaud Vandevelde, Nathalie Monique (2021) JMIR medical informatics — Vol. 9, no.7, p. e27980 [1-10] (2021)