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pro vyhledávání: '"Happle, R.H.G."'
Autor:
Bornholdt, D., Oeffner, F., Konig, A., Happle, R.H.G., Alanay, Y., Ascherman, J., Benke, P.J., Boente Mdel, C., Burgt, I. van der, Chassaing, N., Ellis, I., Francisco, C.R., Giovanna, P. Della, Hamel, B.C.J., Has, C., Heinelt, K., Janecke, A., Kastrup, W., Loeys, B.L., Lohrisch, I., Marcelis, C.L.M., Mehraein, Y., Nicolas, M.E., Pagliarini, D., Paradisi, M., Patrizi, A., Piccione, M., Piza-Katzer, H., Prager, B., Prescott, K., Strien, J., Utine, G.E., Zeller, M.S., Grzeschik, K.H.
Publikováno v:
Human Mutation, 30, 5, pp. E618-28
Human Mutation, 30, E618-28
Human Mutation, 30, E618-28
Contains fulltext : 81709.pdf (Publisher’s version ) (Closed access) The X-linked dominant trait focal dermal hypoplasia (FDH, Goltz syndrome) is a developmental defect with focal distribution of affected tissues due to a block of Wnt signal transm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e5b8f7a9ef9ef149ca41a9173767ca3f
https://hdl.handle.net/2066/81709
https://hdl.handle.net/2066/81709
Publikováno v:
European Journal of Dermatology, 9, pp. 217-219
European Journal of Dermatology, 9, 217-219
European Journal of Dermatology, 9, 217-219
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a3d128d4e1368cc2bcbc97514d0748bc
https://hdl.handle.net/2066/184509
https://hdl.handle.net/2066/184509
Publikováno v:
European Journal of Dermatology, 10, pp. 217-9
European Journal of Dermatology, 10, 217-9
European Journal of Dermatology, 10, 217-9
Item does not contain fulltext 3 p.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f5e4b373ed1d3ba01fa842968713a4c9
https://hdl.handle.net/2066/184647
https://hdl.handle.net/2066/184647
