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Shortcutting the diagnostic odyssey: the multidisciplinary ..:
Schuermans, Nika
;
Hemelsoet, Dimitri
;
Terryn, Wim
...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/s13023-022-02365-y
RT Journal T1
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13023-022-02365-y&Exemplar=1&LAN=DE A1 Schuermans, Nika A1 Hemelsoet, Dimitri A1 Terryn, Wim A1 Steyaert, Sanne A1 Van Coster, Rudy A1 Coucke, Paul J. A1 Steyaert, Wouter A1 Callewaert, Bert A1 Bogaert, Elke A1 Verloo, Patrick A1 Vanlander, Arnaud V. A1 Debackere, Elke A1 Ghijsels, Jody A1 LeBlanc, Pontus A1 Verdin, Hannah A1 Naesens, Leslie A1 Haerynck, Filomeen A1 Callens, Steven A1 Dermaut, Bart A1 Poppe, Bruce A1 De Bleecker, Jan A1 Santens, Patrick A1 Boon, Paul A1 Laureys, Guy A1 Kerre, Tessa A1 for UD-PrOZA PB Springer Science and Business Media LLC YR 2022 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 17 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13023-022-02365-y DO https://doi.org/10.1186/s13023-022-02365-y SF ELIB - SuUB Bremen
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