Zobrazeno 1 - 10
of 99
pro vyhledávání: '"GRZESCHIK, K.H."'
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
Autor:
Károlyi, L., Konrad, M., Köckerling, A., Ziegler, A., Zimmermann, D.K., Roth, B., Wieg, C., Grzeschik, K.H., Koch, M.C., Seyberth, H.W., Vargas, R., Forestier, C., Jean, G., Deschaux, M., Rizzoni, G.F., Niaudet, P., Antignac, C., Feldmann, D., Lorridon, F., Cougoureux, E., Laroze, F., Alessandri, J.-L., David, L., Saunier, P., Deschenes, G., Hildebrandt, F., Vollmer, M., Proesmans, W., Brandis, M., Heuvel, L.P.W.J. van den, Lemmink, H.H., Nillesen, W., Monnens, L.A.H., Knoers, N.V.A.M., Guay-Woodford, L.M., Wright, C.J., Madrigal, G., Hebert, S.C.
Publikováno v:
Human Molecular Genetics, 6, 1, pp. 17-26
Human Molecular Genetics, 6, 17-26
Human Molecular Genetics, 6, 17-26
Contains fulltext : 24466___.PDF (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::17539fb075a7c5472cad4b76e3b64892
https://hdl.handle.net/2066/24466
https://hdl.handle.net/2066/24466
Background CHILD syndrome, a rare hereditary disorder of keratinization (MIM 308050, 300275), is the acronym proposed by Happle to name a rare entity, characterized by congenital hemidysplasia, icthyosiform nevus and limb defects, ranging from digita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c8a8fb07b644e5e0dc33db83dcf8e97d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3130788
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3130788
Autor:
Wiese, S., Emmerich, D., Schröder, B., Murphy, D.B., Grzeschik, K.H., Geurts van Kessel, A.H.M., Thies, U.
Publikováno v:
DNA and Cell Biology, 16, 2, pp. 165-171
DNA and Cell Biology, 16, 165-171
DNA and Cell Biology, 16, 165-171
Contains fulltext : 25058.pdf (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::75c9c9c12e21ddba77aa72ec6b95796d
https://hdl.handle.net/2066/25058
https://hdl.handle.net/2066/25058
Autor:
Oeffner, F., Bornholdt, D., Ziegler, A., Hinney, A., Görg, T., Gerber, G., Goldschmidt, H.P., Siegfried, W., Wright, A., Hebebrand, J., Grzeschik, K.H.
Publikováno v:
Acta Diabetologica; Nov2000, Vol. 37 Issue 2, p93-101, 9p
Publikováno v:
Cytogenetics & Cell Genetics; 1991, Vol. 58 Issue 1/2, p785-799, 15p
Publikováno v:
Cytogenetics & Cell Genetics; 1990, Vol. 55 Issue 1-4, p229-234, 6p
Autor:
Gerald, P.S., Grzeschik, K.H.
Publikováno v:
Cytogenetics & Cell Genetics; 1984, Vol. 37 Issue 1-4, p103-126, 24p
Autor:
WIESE, S., EMMERICH, D., SCHRÖDER, B., MURPHY, D.B., GRZESCHIK, K.H., VAN KESSEL, A. GEURTS, THIES, U.
Publikováno v:
DNA & Cell Biology; Feb1997, Vol. 16 Issue 2, p165-171, 7p
Autor:
Braun, T., Bober, E., Buschhausen‐Denker, G., Kohtz, S., Grzeschik, K.H., Arnold, H.H., Kotz, S.
Publikováno v:
The EMBO Journal; December 1989, Vol. 8 Issue: 12 p3617-3625, 9p