Search | DIAL.pr - BOREAL

Accès à distance ? S'identifier sur le proxy UCLouvain

Displaying 3 results.

- Journal article
Destructive juvenile idiopathic arthritis: do not overlook rare genetic skeletal disorders
Triaille, Clément[UCL] Vanhoenacker, Filip M Mortier, Geert R (2021) The Lancet. Rheumatology — Vol. 3, no.6, p. e404 (2021)
- Journal article
Corrigendum: Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium.
Laurent, Michaël R De Schepper, Jean Trouet, Dominique Godefroid, Nathalie[UCL] Boros, Emese Heinrichs, Claudine Bravenboer, Bert Velkeniers, Brigitte Lammens, Johan Harvengt, Pol Cavalier, Etienne Kaux, Jean-François Lombet, Jacques De Waele, Kathleen Verroken, Charlotte van Hoeck, Koenraad Mortier, Geert R Levtchenko, Elena Vande Walle, Johan (2021) Frontiers in endocrinology — Vol. 12, p. 686401 [1-2] (2021)
- Journal article
Heterozygous pathogenic variants involving cause a new skeletal disorder resembling cleidocranial dysplasia.
Beyltjens, Tessi Boudin, Eveline Revencu, Nicole[UCL] Boeckx, Nele Bertrand, Miriam Schütz, Leon Haack, Tobias B Weber, Axel Biliouri, Eleni Vinkšel, Mateja Zagožen, Anja Peterlin, Borut Pai, Shashidhar Telegrafi, Aida Henderson, Lindsay B Ells, Courtney Turner, Lesley Wuyts, Wim Van Hul, Wim Hendrickx, Gretl Mortier, Geert R (2023) Journal of medical genetics — Vol. 60, no. 5, p. 498-504 (2023)