Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome von Delbaere, Sarah, Van Damme, Tim, Syx, Delfien, Symoens, Sofie, Coucke, Paul, Willaert, Andy, Malfait, Fransiska

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Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder von Malfait, Fransiska, Kariminejad, Ariana, Van Damme, Tim, Gauche, Caroline, Syx, Delfien, Merhi-Soussi, Faten, Gulberti, Sandrine, Symoens, Sofie, Vanhauwaert, Suzanne, Willaert, Andy, Bozorgmehr, Bita, Kariminejad, Mohamad Hasan, Ebrahimiadib, Nazanin, Hausser, Ingrid, Huysseune, Ann, Fournel-Gigleux, Sylvie, De Paepe, Anne

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More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome von Dhooge, Tibbe, Van Damme, Tim, Syx, Delfien, Mosquera, Laura M., Nampoothiri, Sheela, Radhakrishnan, Anil, Simsek‐Kiper, Pelin O., Utine, Gülen E., Bonduelle, Maryse, Migeotte, Isabelle, Essawi, Osama, Ceylaner, Serdar, Al Kindy, Adila, Tinkle, Brad, Symoens, Sofie, Malfait, Fransiska

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The Ehlers-Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism von Van Damme, Tim, Colman, Marlies, Syx, Delfien, Malfait, Fransiska

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Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis von Syx, Delfien, Van Damme, Tim, Symoens, Sofie, Maiburg, Merel C., van de Laar, Ingrid, Morton, Jenny, Suri, Mohnish, Del Campo, Miguel, Hausser, Ingrid, Hermanns-Lê, Trinh, De Paepe, Anne, Malfait, Fransiska

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa von Van Damme, Tim, Gardeitchik, Thatjana, Mohamed, Miski, Guerrero-Castillo, Sergio, Freisinger, Peter, Guillemyn, Brecht, Kariminejad, Ariana, Dalloyaux, Daisy, van Kraaij, Sanne, Lefeber, Dirk J., Syx, Delfien, Steyaert, Wouter, De Rycke, Riet, Hoischen, Alexander, Kamsteeg, Erik-Jan, Wong, Sunnie Y., van Scherpenzeel, Monique, Jamali, Payman, Brandt, Ulrich, Nijtmans, Leo, Korenke, G. Christoph, Chung, Brian H.Y., Mak, Christopher C.Y., Hausser, Ingrid, Kornak, Uwe, Fischer-Zirnsak, Björn, Strom, Tim M., Meitinger, Thomas, Alanay, Yasemin, Utine, Gulen E., Leung, Peter K.C., Ghaderi-Sohi, Siavash, Coucke, Paul, Symoens, Sofie, De Paepe, Anne, Thiel, Christian, Haack, Tobias B., Malfait, Fransiska, Morava, Eva, Callewaert, Bert, Wevers, Ron A.

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Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review von D'hondt, Sanne, Van Damme, Tim, Malfait, Fransiska

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Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome von Van Damme, Tim, Pang, Xiaomeng, Guillemyn, Brecht, Gulberti, Sandrine, Syx, Delfien, De Rycke, Riet, Kaye, Olivier, de Die-Smulders, Christine E M, Pfundt, Rolph, Kariminejad, Ariana, Nampoothiri, Sheela, Pierquin, Geneviève, Bulk, Saskia, Larson, Austin A, Chatfield, Kathryn C, Simon, Marleen, Legrand, Anne, Gerard, Marion, Symoens, Sofie, Fournel-Gigleux, Sylvie, Malfait, Fransiska

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Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta von Syx, Delfien, Ishikawa, Yoshihiro, Gebauer, Jan, Boudko, Sergei P, Guillemyn, Brecht, Van Damme, Tim, D'hondt, Sanne, Symoens, Sofie, Nampoothiri, Sheela, Gould, Douglas B, Baumann, Ulrich, Bächinger, Hans Peter, Malfait, Fransiska

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The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review von Colman, Marlies, Van Damme, Tim, Steichen-Gersdorf, Elisabeth, Laccone, Franco, Nampoothiri, Sheela, Syx, Delfien, Guillemyn, Brecht, Symoens, Sofie, Malfait, Fransiska

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Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type von Van Damme, Tim, Colige, Alain, Syx, Delfien, Giunta, Cecilia, Lindert, Uschi, Rohrbach, Marianne, Aryani, Omid, Alanay, Yasemin, Simsek-Kiper, Pelin Özlem, Kroes, Hester Y., Devriendt, Koen, Thiry, Marc, Symoens, Sofie, De Paepe, Anne, Malfait, Fransiska

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Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6‐deficient spondylodysplastic Ehlers–Danlos syndrome von Nikpour, Mahnaz, Noborn, Fredrik, Nilsson, Jonas, Van Damme, Tim, Kaye, Olivier, Syx, Delfien, Malfait, Fransiska, Larson, Göran

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Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review von D'hondt, Sanne, Van Damme, Tim, Malfait, Fransiska

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Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome : a systematic review von D'hondt, Sanne, Van Damme, Tim, Malfait, Fransiska

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The Ehlers–Danlos syndromes against the backdrop of inborn errors of metabolism von Van Damme, Tim, Colman, Marlies, Syx, Delfien, Malfait, Fransiska

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RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder von Santens, Patrick, Van Damme, Tim, Steyaert, Wouter, Willaert, Andy, Sablonnière, Bernard, De Paepe, Anne, Coucke, Paul J, Dermaut, Bart

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Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations von Vanbelleghem, Eva, Van Damme, Tim, Beyens, Aude, Symoens, Sofie, Claes, Kathleen, De Backer, Julie, Meerschaut, Ilse, Vanommeslaeghe, Floris, Delanghe, Sigurd E, van den Ende, Jenneke, Beyltjens, Tessi, Scimone, Eleanor R, Lindsay, Mark E, Schimmenti, Lisa A, Hinze, Alicia M, Dunn, Emily, Gomez-Ospina, Natalia, Vandernoot, Isabelle, Delguste, Thomas, Coppens, Sandra, Cormier-Daire, Valérie, Tartaglia, Marco, Garavelli, Livia, Shieh, Joseph, Demir, Şenol, Arslan Ateş, Esra, Zenker, Martin, Rohanizadegan, Mersedeh, Rivera-Cruz, Greysha, Douzgou, Sofia, Lin, Angela E, Callewaert, Bert

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Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta von Syx, Delfien, Ishikawa, Yoshihiro, Gebauer, Jan, Boudko, Sergei P, Guillemyn, Brecht, Van Damme, Tim, D'hondt, Sanne, Symoens, Sofie, Nampoothiri, Sheela, Gould, Douglas B, Baumann, Ulrich, Bachinger, Hans Peter, Malfait, Fransiska

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Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations von Vanbelleghem, Eva, Van Damme, Tim, Beyens, Aude, Symoens, Sofie, Claes, Kathleen, De Backer, Julie, Meerschaut, Ilse, Vanommeslaeghe, Floris, Delanghe, Sigurd E, van den Ende, Jenneke, Beyltjens, Tessi, Scimone, Eleanor R, Lindsay, Mark E, Schimmenti, Lisa A, Hinze, Alicia M, Dunn, Emily, Gomez-Ospina, Natalia, Vandernoot, Isabelle, Delguste, Thomas, Coppens, Sandra, Cormier-Daire, Valérie, Tartaglia, Marco, Garavelli, Livia, Shieh, Joseph, Demir, Şenol, Arslan Ateş, Esra, Zenker, Martin, Rohanizadegan, Mersedeh, Rivera-Cruz, Greysha, Douzgou, Sofia, Lin, Angela E, Callewaert, Bert

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Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay von Baert, Annelot, Depuydt, Julie, Van Maerken, Tom, Poppe, Bruce, Malfait, Fransiska, Van Damme, Tim, De Nobele, Sylvia, Perletti, Gianpaolo, De Leeneer, Kim, Claes, Kathleen B M, Vral, Anne

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