المؤلفون: Sergouniotis, Panagiotis I., Maxime, Emmanuel, Leroux, Dorothée, Olry, Annie, Thompson, Rachel, Rath, Ana, Robinson, Peter N., Dollfus, HélèneAshworth JL, Audo I, Balciuniene VJ, Banin E, Black GC, Böhringer D, Boon CJF, Bremond-Gignac D, Calvas P, Castela G, Dagnelie G, Dollfus H, Downes SM, Fasolo A, Fasser C, Gelzinis A, Goetz K, Hamann S, Héon E, Iarossi G, Kawasaki A, Keegan D, Kessel L, Khan K, Klett A, Köhler S, Leroux D, Leroy BP, Lisch W, Liskova P, Lorenz B, Maggi R, Maxime E, Meunier I, Mohand-Said S, Nowomiejska K, Perdomo Y, Petzold A, Preising M, Robinson PN, Scholl HPN, Sergouniotis PI, Sodi A, Stingl K, Studer F, Suppiej A, Thompson R, Touitou V, Traboulsi E, Trumpaitis J, Tuft SJ, Vaclavik V, Valeina S, Van Cauwenbergh C, Verloes A, Vighetto A, Wheeler R, Wheeler-Schilling T, Yu-Wai-Man P, Zobor D, Zrenner E.

المساهمون: Sergouniotis, Panagiotis I., Maxime, Emmanuel, Leroux, Dorothée, Olry, Annie, Thompson, Rachel, Rath, Ana, Robinson, Peter N., Dollfus, Hélèneashworth, Jl, Audo, I, Balciuniene, Vj, Banin, E, Black, Gc, Böhringer, D, Boon, Cjf, Bremond-Gignac, D, Calvas, P, Castela, G, Dagnelie, G, Dollfus, H, Downes, Sm, Fasolo, A, Fasser, C, Gelzinis, A, Goetz, K, Hamann, S, Héon, E, Iarossi, G, Kawasaki, A, Keegan, D, Kessel, L, Khan, K, Klett, A, Köhler, S, Leroux, D, Leroy, Bp, Lisch, W, Liskova, P, Lorenz, B, Maggi, R, Maxime, E, Meunier, I, Mohand-Said, S, Nowomiejska, K, Perdomo, Y, Petzold, A, Preising, M, Robinson, Pn, Scholl, Hpn, Sergouniotis, Pi, Sodi, A, Stingl, K, Studer, F, Suppiej, A, Thompson, R, Touitou, V, Traboulsi, E, Trumpaitis, J, Tuft, Sj, Vaclavik, V, Valeina, S, Van Cauwenbergh, C, Verloes, A, Vighetto, A, Wheeler, R, Wheeler-Schilling, T, Yu-Wai-Man, P, Zobor, D, Zrenner, E.

مصطلحات موضوعية: Evidence-based precision medicine, Rare eye disease, Human phenotype ontology, Orphanet rare disease ontology

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/30626441; info:eu-repo/semantics/altIdentifier/wos/WOS:000455361900003; volume:14; issue:1; firstpage:8-1; lastpage:8-5; numberofpages:5; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/11392/2400086; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85059797765; https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0980-6

الاتاحة: http://hdl.handle.net/11392/2400086
https://doi.org/10.1186/s13023-018-0980-6
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0980-6