Showing 1 - 7 results of 7 for search 'Wieczorek D.', query time: 0.04s
Refine Results
-
1
Original Model for Estimating the Whole Life Costs of Buildings and its Verification by Plebankiewicz E., Zima K., Wieczorek D.
Published 2019-06-01
Article -
2
Life Cycle Cost Modelling of Buildings with Consideration of the Risk by Plebankiewicz E., Zima K., Wieczorek D.
Published 2016-06-01
Article -
3
Identification of mutations in TXNL4A in Burn-McKeown Syndrome and isolated choanal atresia by Goos, J, Swagemakers, S, Twigg, S, van Dooren, M, Hoogeboom, A, Beetz, C, Günther, S, Magielsen, F, Ockeloen, C, Ramos-Arroyo, M, Pfundt, R, Yntema, H, van der Spek, P, Stanier, P, Wieczorek, D, Wilkie, A, van den Ouweland, A, Mathijssen, I, Hurst, J
Published 2017Journal article -
4
Mutations in MAP3K7 that alter the activity of the TAK1 signaling complex cause frontometaphyseal dysplasia. by Wade, E, Daniel, P, Jenkins, Z, McInerney-Leo, A, Morgan, T, Addor, M, Ades, L, Bertola, D, Bohring, A, Carter, E, Cho, T, Duba, H, Fletcher, E, Kim, C, Krakow, D, Morava, E, Neuhann, T, Superti-Furga, A, Veenstra-Knol, I, Wieczorek, D, Wilson, L, Hennekam, R, Sutherland-Smith, A, Strom, T, Wilkie, A, Brown, M, Duncan, E, Markie, D, Robertson, S
Published 2016Journal article -
5
Mutations in the BAF-complex subunit DPF2 associated with Coffin-Siris syndrome by Vasileiou, G, Vergarajauregui, S, Endele, S, Popp, B, Büttner, C, Ekici, AB, Gerard, M, Bramswig, NC, Albrecht, B, Clayton-Smith, J, Morton, J, Tomkins, S, Low, K, Weber, A, Wenzel, M, Altmüller, J, Li, Y, Wollnik, B, Hoganson, G, Plona, MR, Cho, MT, Thiel, CT, Lüdecke, HJ, Strom, TM, Calpena, E, Wilkie, AOM, Wieczorek, D, Engel, FB, Reis, A
Published 2018Journal article -
6
Mutations in MAP3K7 that alter the activity of the TAK1 signaling complex cause frontometaphyseal dysplasia by Wade, E, Daniel, P, Jenkins, Z, McInerney-Leo, A, Leo, P, Morgan, T, Addor, M, Adès, L, Bertola, D, Bohring, A, Carter, E, Cho, T, Duba, H, Fletcher, E, Kim, C, Krakow, D, Morava, E, Neuhann, T, Superti-Furga, A, Veenstra-Knol, I, Wieczorek, D, Wilson, L, Hennekam, R, Sutherland-Smith, A, Strom, T, Wilkie, A, Brown, M, Duncan, E, Markie, D, Robertson, S
Published 2016Journal article -
7
ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome by Zak, J, Vives, V, Szumska, D, Vernet, A, Schneider, J, Miller, P, Slee, E, Joss, S, Lacassie, Y, Chen, E, Escobar, L, Tucker, M, Aylsworth, A, Dubbs, H, Collins, A, Andrieux, J, Dieux-Coeslier, A, Haberlandt, E, Kotzot, D, Scott, D, Parker, M, Zakaria, Z, Choy, Y, Wieczorek, D, Innes, A, Jun, K, Zinner, S, Prin, F, Lygate, C, Pretorius, P, Rosenfeld, J, Mohun, T, Lu, X
Published 2016Journal article