Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Caroline van Mourik"'
Autor:
Marianne Rohrbach, Tim Van Damme, Serwet Demirdas, Sylvie Fournel-Gigleux, Angela F. Brady, Johannes Zschocke, Neeti Ghali, Tomoki Kosho, Cecilia Giunta, Nicol C. Voermans, Fransiska Malfait, Anthony Vandersteen, Caroline van Mourik, Ines Kapferer-Seebacher, Roberto Mendoza-Londono, Michael F. Pope
Publikováno v:
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 1, pp. 70-115
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2017, 175 (1), pp.70-115. ⟨10.1002/ajmg.c.31550⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 70-115
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 175(1), 70-115. Wiley-Liss Inc.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2017, 175 (1), pp.70-115. ⟨10.1002/ajmg.c.31550⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 70-115
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 175(1), 70-115. Wiley-Liss Inc.
Item does not contain fulltext The Ehlers-Danlos syndromes comprise a clinically and genetically heterogeneous group of heritable connective tissue disorders, which are characterized by joint hypermobility, skin hyperextensibility, and tissue friabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255d39b12dc10996bc815e347b5c6496
https://pubmed.ncbi.nlm.nih.gov/28306225
https://pubmed.ncbi.nlm.nih.gov/28306225
Autor:
Brad T. Tinkle, Tomoki Kosho, Clair A. Francomano, Eyal Reinstein, Neeti Ghali, Jessica M Bowen, Johannes Zschocke, Marianne Rohrbach, James H. Black, Roberto Mendoza-Londono, Michael Frank, Marco Castori, Serwet Demirdas, Angela F. Brady, Helen Cohen, Diana Johnson, Nicol C. Voermans, Birgit Juul-Kristensen, F. Michael Pope, Mark E. Lavallee, Sylvie Fournel-Gigleux, John W. Belmont, Nigel Wheeldon, Anne De Paepe, Rodney Grahame, Fransiska Malfait, Cecilia Giunta, Peter H. Byers, Leema Robert, Ines Kapferer-Seebacher, Nigel Burrows, Anthony Vandersteen, Caroline van Mourik, Melanie Pepin, Lara Bloom, Glenda Sobey, Howard P. Levy, Tim Van Damme, Britta Berglund, Lynn Sanders, Marina Colombi, Alan Hakim, Hanadi Kazkaz, Xavier Jeunemaitre, Julie De Backer
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 1, pp. 8-26
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 8-26
Malfait, F, Francomano, C, Byers, P H, Belmont, J, Berglund, B, Black, J, Bloom, L, Bowen, J M, Brady, A F, Burrows, N P, Castori, M, Cohen, H, Colombi, M, Demirdas, S, De Backer, J, De Paepe, A, Fournel-Gigleux, S, Frank, M, Ghali, N, Giunta, C, Grahame, R, Hakim, A, Jeunemaitre, X, Johnson, D, Juul-Kristensen, B, Kapferer-Seebacher, I, Kazkaz, H, Kosho, T, Lavallee, M E, Levy, H, Mendoza-Londono, R, Pepin, M, Pope, F M, Reinstein, E, Robert, L, Rohrbach, M, Sanders, L, Sobey, G J, Van Damme, T, Vandersteen, A, van Mourik, C, Voermans, N, Wheeldon, N, Zschocke, J & Tinkle, B 2017, ' The 2017 international classification of the Ehlers-Danlos syndromes ', American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, vol. 175, no. 1, pp. 8-26 . https://doi.org/10.1002/ajmg.c.31552
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 1, pp. 8-26
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 8-26
Malfait, F, Francomano, C, Byers, P H, Belmont, J, Berglund, B, Black, J, Bloom, L, Bowen, J M, Brady, A F, Burrows, N P, Castori, M, Cohen, H, Colombi, M, Demirdas, S, De Backer, J, De Paepe, A, Fournel-Gigleux, S, Frank, M, Ghali, N, Giunta, C, Grahame, R, Hakim, A, Jeunemaitre, X, Johnson, D, Juul-Kristensen, B, Kapferer-Seebacher, I, Kazkaz, H, Kosho, T, Lavallee, M E, Levy, H, Mendoza-Londono, R, Pepin, M, Pope, F M, Reinstein, E, Robert, L, Rohrbach, M, Sanders, L, Sobey, G J, Van Damme, T, Vandersteen, A, van Mourik, C, Voermans, N, Wheeldon, N, Zschocke, J & Tinkle, B 2017, ' The 2017 international classification of the Ehlers-Danlos syndromes ', American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, vol. 175, no. 1, pp. 8-26 . https://doi.org/10.1002/ajmg.c.31552
Item does not contain fulltext The Ehlers-Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f0b002b28d94b1fa69a6762a4a7db7
https://www.zora.uzh.ch/id/eprint/145775/
https://www.zora.uzh.ch/id/eprint/145775/
