A qualitative study among patients with an inherited retinal disease on the meaning of genomic unsolicited findings

par Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Caroline Van Cauwenbergh, Bart P. Leroy, Ignaas Devisch, Elfride De Baere
Publié 2021

Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes

par Delfien J. Bogaert, Melissa Dullaers, Hye Sun Kuehn, Bart P. Leroy, Julie E. Niemela, Hans De Wilde, Sarah De Schryver, Marieke De Bruyne, Frauke Coppieters, Bart N. Lambrecht, Frans De Baets, Sergio D. Rosenzweig, Elfride De Baere, Filomeen Haerynck
Publié 2017