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Ehlers-Danlos syndrome, hypermobility type, is linked to chromosome 8p22-8p21.1 in an extended Belgian family

Syx, Delfien, Symoens, Sofie, Steyaert, Wouter, De Paepe, Anne, Coucke, Paul, Malfait, Fransiska
2015

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Flemish network on rare connective tissue diseases (CTD) : patient pathways in systemic sclerosis : first steps taken

Piette, Yves, Van den Bossche, Freek, Aerts, J., Aerts, N., Ajeganova, S., Badot, V., Berghen, N., Blockmans, D., Brusselle, Guy, Caeyers, N., De Decker, Melissa, De Haes, P., De Cock, C., De Keyser, F., De Langhe, E., Delcroix, M., De Nutte, H., De Pauw, Martine, Depicker, A., De Sutter, An, De Sutter, J., Du Four, Tessa, Frank, C., Goubau, J., Guiot, J., Gutermuth, J., Heeman, L., Houssiau, F., Hennes, I., Lenaerts, J., Lintermans, A., Loeys, B., Luyten, H., Maeyaert, B., Malfait, Fransiska, Moeyersoons, A., Mostmans, Y., Nijs, J., Poppe, B., Polfliet, K., Ruttens, D., Sabato, V., Schoeters, E., Slabbynck, H., Stuer, A., Tamirou, F., Thevissen, Kristof, Van Kersschaever, G., Vanneuville, B., Van Offel, J., Vanthuyne, M., Van Wabeke, J., Verbist, C., Vos, I., Westhovens, R., Wuyts, W., Yserbyt, J., Smith, Vanessa
2024