Zobrazeno 1 - 10
of 244
pro vyhledávání: '"Z, Tümer"'
Autor:
S.M. White, R. Mollicone, M. Rozek, Z. Tümer, T. Opiola, J.-J. Candelier, C.R. Bonvicino, H. Winking, A. Hebinck, H. Kuiper, Ch. Zühlke, H. Yasue, J.M. Perez de la Lastra, S. Kiuchi, A. Pienkowska, N. Arnal, B. Gläser, C. Ngo, H. Mehenni, C. Steinlein, P.S. D’Andrea, R.P.M.A. Crooijmans, A. Eggen, C. Zijlstra, M. Yerle, U. Butzmann, S.E. Antonarakis, Y.E. Shahein, E. Anton, R. Korstanje, D.F. de Andres-Cara, N.A. de Haan, R. Heilig, B. Brenig, J. Egozcue, C. Delcros, M. Østergaard, G.F. Gillissen, A. Wandall, R. Kreutz, R.J. McKinlay Gardner, F. Piumi, M. Mahony, A. Robic, C. Ozouf-Costaz, N. Tommerup, T. Haaf, C. Rodellar, C. Szpirer, F. Vidal, P.A. Ioannou, P.M. Kroisel, C. Drögemüller, K. Buchet-Poyau, Y. Takagaki, T.L. Harboe, C. Wilhelm, F. Porto-Foresti, J. Barciszewski, A.C.M. Bonné, M.T. Roldan-Arjona, C. Rogel-Gaillard, H. Hiraiwa, Y. Muneta, M. Grzmil, P. Zaragoza, C. Bonillo, H.A. van Lith, J. Kunz, A. Dalski, O. Distl, F. Laccone, D. Milan, C. Windpassinger, T. Awata, H. Uenishi, J. Szpirer, R. Fries, A.A. Bosma, F. Foresti, M.F.Z. Daniel-Silva, H. Hayes, R. Roy, H. Omran, P. Pinton, S. Schlickum, E. Petek, E. Schwinger, L. Li, P. Coullin, C. Knorr, L.F.M. van Zutphen, J. Blanco, H.P. Klinger, A. Volz, J. Mißbach, I.B. Otazu, E. Northrop, C. Andersen, P. Burfeind, M. Den Bieman, M. Meins, R. Melkaoui, J. Beck, U. Radhakrishna, M. Gautier, R. Oriol, L.F. Almeida-Toledo, I. Nanda, K. Wagner, F. Habermann, V. Petrovic, M. Schmid, R. Yamamoto, P. Moore, P. van Vooren, G. Hauke, H. Zürcher, F. Hildebrandt, C.G. Ziegler, J. Koch, P. Laurent, J.L. Williams, M.A.M. Groenen, J.J. Garrido, C. Schelling, S. Yadav, C. Kosan, H.R. Slater
Publikováno v:
Cytogenetic and Genome Research. 97:261-275
Autor:
L, Roos, M, Fang, C, Dali, H, Jensen, N, Christoffersen, B, Wu, J, Zhang, R, Xu, P, Harris, X, Xu, K, Grønskov, Z, Tümer
Publikováno v:
Clinical genetics. 86(3)
Anomalies of eye development can lead to the rare eye malformations microphthalmia and anophthalmia (small or absent ocular globes), which are genetically very heterogeneous. Several genes have been associated with microphthalmia and anophthalmia, an
This Book/Chapter has been retracted as the rights have been returned to the author. The full Elsevier Policy on Book/Chapter Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef749af685907a9f9ed6cab8b00e58c3
https://doi.org/10.1016/b978-0-12-404613-9.00013-7
https://doi.org/10.1016/b978-0-12-404613-9.00013-7
This Book/Chapter has been retracted as the rights have been returned to the author. The full Elsevier Policy on Book/Chapter Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b90f59f6eb7f71ae7ccbd5fc72c26d
https://doi.org/10.1016/b978-0-12-404613-9.00028-9
https://doi.org/10.1016/b978-0-12-404613-9.00028-9
Autor:
N D, Rendtorff, I, Schrijver, M, Lodahl, J, Rodriguez-Paris, T, Johnsen, E C, Hansén, L A A, Nickelsen, Z, Tümer, T, Fagerheim, R, Wetke, L, Tranebjaerg
Publikováno v:
Clinical genetics. 84(4)
Autor:
E. Petek, M. Rozek, Z. Tümer, S.E. Antonarakis, E. Anton, Ch. Zühlke, J.L. Williams, U. Butzmann, M.A.M. Groenen, E. Northrop, A.C.M. Bonné, J.M. Perez de la Lastra, H.R. Slater, N.A. de Haan, R. Heilig, C. Delcros, Y.E. Shahein, J.J. Garrido, F. Porto-Foresti, M. Østergaard, C. Steinlein, A. Robic, G.F. Gillissen, A. Volz, R.J. McKinlay Gardner, T.L. Harboe, B. Brenig, R. Korstanje, S.M. White, M. Den Bieman, R. Melkaoui, R. Kreutz, F. Piumi, J. Beck, D.F. de Andres-Cara, T. Haaf, C. Rodellar, U. Radhakrishna, M. Gautier, N. Tommerup, K. Wagner, I. Nanda, K. Buchet-Poyau, L.F. Almeida-Toledo, P.S. D’Andrea, P.M. Kroisel, M. Grzmil, C. Schelling, M. Mahony, C. Drögemüller, J. Barciszewski, M. Meins, F. Vidal, C. Zijlstra, S. Yadav, C. Bonillo, C. Kosan, V. Petrovic, J. Egozcue, F. Habermann, M. Schmid, R. Roy, A.A. Bosma, F. Foresti, C. Windpassinger, H. Uenishi, R. Yamamoto, H. Hiraiwa, A. Dalski, R. Mollicone, J. Szpirer, R. Fries, C. Wilhelm, R. Oriol, C. Ozouf-Costaz, M.F.Z. Daniel-Silva, H. Hayes, E. Schwinger, P. Coullin, C. Andersen, P. Pinton, M.T. Roldan-Arjona, C. Rogel-Gaillard, J.-J. Candelier, L.F.M. van Zutphen, H.A. van Lith, P.A. Ioannou, O. Distl, H. Omran, J. Kunz, S. Schlickum, T. Awata, L. Li, H. Kuiper, H.P. Klinger, P. van Vooren, S. Kiuchi, J. Mißbach, N. Arnal, A. Pienkowska, D. Milan, C. Ngo, H. Mehenni, R.P.M.A. Crooijmans, T. Opiola, B. Gläser, I.B. Otazu, C.R. Bonvicino, H. Winking, A. Hebinck, J. Blanco, A. Eggen, A. Wandall, C. Knorr, C. Szpirer, H. Zürcher, F. Hildebrandt, C.G. Ziegler, Y. Takagaki, J. Koch, P. Laurent, P. Burfeind, H. Yasue, P. Moore, M. Yerle, G. Hauke, Y. Muneta, P. Zaragoza, F. Laccone
Publikováno v:
Cytogenetic and Genome Research. 97:281-283
Autor:
S. Ohta, D. Simon, J.H. Kurth, C.N. Hahn, B.K. May, M.C. Kurth, I. Rodriguez de Ledesma, Y.D. Patel, C. Steinlein, B.D. Harris, J.P. Banga, S. Mazan, B. Weiffenbach, D.S. Gallagher, O.M. Garson, J.E. Womack, Z. Tümer, H. Nishi, H.M. Kozman, E.J.M. Schuurman, T. Sasazuki, N. Aoki, A. Pellicer, H.A. Phillips, A.A.B. Bergen, G.J.B. van Ommen, J.C. Mulley, J.A. Padilla, A. Kato, C. Jeanpierre, N. Roeckel, A.P. Monaco, C. Rudduck, D. Sheer, T.A. Jones, E. Austruy, C. Junien, R. Espinosa, A.M. Ryan, G.R. Sutherland, J.-P. Bachellerie, Ca. Westbrook, M. Schmid, H. Lerach, E. Dietzsch, A. Rabasco, D.F. Callen, L. Sottrup-Jensen, M. Cohen-Salmon, T. Kristensen, M M Le Beau, S. Hirosawa, A.M. McGregor, J.J. Pérez-Regadera, E. Bakker, P. Laslo, J.L. Fernández-García, L.-H. Qu, M.C. Wapenaar, M. Dixon, L.M. Duncan, R.H. Martin, R.I. Barnes, A. Kimura, E.M. Bleeker-Wagemakers, A.M. Bowcock, S.A. Whitmore, N. Tommerup, B.B. Knowles, J. Santos, J.L. Omdahl, W.L. Neuman, M. Guttenbach, A.N. Silahtaroglu, P.S. Barnett, M.-G. Mattéi, L. Iannuzzi, Y. Nakamura, E. Baker, P.J. Diergaarde, G.P. Di Meo, M. Martínez-Trancón, S. Toyota
Publikováno v:
Cytogenetic and Genome Research. 62:I-IV
Autor:
B. Rosenbusch, M.-T. Bihoreau, J. Satrústegui, J. Browne, B.P. Morgan, C. Niehrs, V.A. Valentine, L.Z. Topol, K. Rader, S.-Y. Li, S. Seino, T. Ono, M.L. Ramírez-Dueñas, K.C Arden, T.-H. Hsu, M. Schmid, S. Rensen, S.H. Park, M.J. Pettenati, H. Yano, W. Van Hul, J.L Vernon, K. Ellington, S. Yonezawa, M.A. Sims, A. Dutra, G. Kandala, S. Paradisi, N.A. Jenkins, F. Gruetzner, C. Dixkens, A.I. Protopopov, N.G. Copeland, A. Glinka, L. Ferretti, H.-U.G. Weier, S. Zabel, Y.-C. Li, S. Sonta, R.A. White, E. Roessler, C. Von Kap-Herr, D. Incarnato, M. Osaki, A. Solans, A.V. Zelenin, E. Petek, G.P. Zambetti, K. Wagner, D.S. Holt, P.M. Richardson, N.D. Rendtorff, T.A. Lister, D. Taruscio, L. Iannuzzi, A. Buck, N.A. Jensen, M.G. Foti, M.A. Hyatt, I. Nanda, M.R. James, P. Doevendans, L. Cai, Y. Du, C.X. George, S. Doerr, M. Athanasiou, G.J.J.M. van Eys, Y. Yokoyama, M.R. Barnes, C.E. Samuel, W. Wuyts, R.S. Bora, M.G. Farquhar, F. Sablitzky, L. Archangelo, M.-G. Mattéi, E.R. Zabarovsky, Q. Zhang, M.-J. Pébusque, M.L. Ayala-Madrigal, L.M. Pasztor, M.-C. Hernandez, R.A. Lersch, S. Yamashita, N. Spurr, G.K. Zoraqi, Y.M. Heng, P.M. Kroisel, M.J. Neat, P. Zambonelli, S. Comincini, R.K. Gupta, G.P. Di Meo, P. Musilová, H. Vissing, Z. Shan, E. Kalm, X. Estivill, S.S. Mann, C. Hansen, I. Hansmann, V. Setaluri, A. Stratil, V.I. Kashuba, R. Davoli, M. Fox, C.C. Lin, H. Egger, J.E. Wiley, Y. Wang, Z. Gu, A. Oohira, A.S. Hill, R. Sanz, V. Falbo, J. Fitzgibbon, P.D. Thomsen, A. Perucatti, J.B. Rattner, G. Merkx, H. Kim, S. Masaki, S. de la Luna, T.L. Harboe, L. Schibler, M.A. Israel, S. Paul, O. Bögler, R.Z. Gizatullin, O.V. Muravenko, B. Brenig, S. Ichikawa, M. Muenke, M.B. Powell, J.-F. Cheng, J. Rubeš, C. Looft, A. Vortkamp, P.C. Burr, T.C. Hart, C. Ramos, N. Tommerup, D.A. Campbell, C.M. Owczarek, B.U. Koelsch, L. Jones, Y. Hirabayashi, K.J. Portbury, S. Aono, C.-Z. Wang, S.D. Field, V. Russo, T. Haaf, P.J. Andres-Barquin, W. Emberger, S. Hirano, C. Lee, A. Kindler-Röhrborn, C. Ayuso, T. Tsukasaki, C. Windpassinger, P.J. Hertzog, A. Kanamori, C. Popovici, A.D. Boyer, M.A. Farwell, N. Foot, L.I. Zon, S. Cepica, D. Birnbaum, A. Silahtaroglu, I. Kola, B. Castiglioni, J. Kohlhase, A. Geurts van Kessel, D.J. Gilbert, M. Yerle, V.W. Sykes, K.E. Murphy, A. del Arco, M. Schneider, E.P. Cribiu, N.K. Rushmere, S.T. Suzuki, S. Breitweser, D.G. Blair, Y.K. Jung, N. Shaikh, Z. Tümer, N. Yokoi, K. Lindpaintner, D.G. Jo
Publikováno v:
Cytogenetic and Genome Research. 89:287-289
Autor:
Z, Tümer, A M, Henriksen, I, Bache, K, Brixen, V, Kalscheuer, V, Kalschauer, N, Illum, K, Rasmussen, L A, Larsen, N, Tommerup
Publikováno v:
Am J Med Genet A
Tümer, Z, Henriksen, A M, Bache, I, Larsen, L A, Tommerup, N, Brixen, K, Kalschauer, V, Illum, N & Rasmussen, K 2005, ' Eponymous Jacobsen Syndrome: Mapping the Breakpoints of the Original Family Suggests an Association Between the Distal 1.1. Mb of Chromosome 21 and Osteoporosis in Down Syndrome ', American Journal of Medical Genetics. Part A, vol. 135, no. 3, pp. 339-341 . https://doi.org/10.1002/ajmg.a.30735
Tümer, Z, Henriksen, A M, Bache, I, Larsen, L A, Tommerup, N, Brixen, K, Kalschauer, V, Illum, N & Rasmussen, K 2005, ' Eponymous Jacobsen Syndrome: Mapping the Breakpoints of the Original Family Suggests an Association Between the Distal 1.1. Mb of Chromosome 21 and Osteoporosis in Down Syndrome ', American Journal of Medical Genetics. Part A, vol. 135, no. 3, pp. 339-341 . https://doi.org/10.1002/ajmg.a.30735
Z. Tumer,* A.M. Henriksen, I. Bache, K. Brixen, V. Kalscheuer, N. Illum, K. Rasmussen, L.A. Larsen, and N. Tommerup Department of Medical Biochemistry and Genetics, Wilhelm Johannsen Centre for Functional Genome Research, The Panum Institute, Univers