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Results: 5

Authors: Gecz, J Mulley, J
Citation: J. Gecz et J. Mulley, Genes for cognitive function: Developments on the X, GENOME RES, 10(2), 2000, pp. 157-163

Authors: Fryns, JP Borghgraef, M Brown, TW Chelly, J Fisch, GS Hamel, B Hanauer, A Lacombe, D Luo, L MacPherson, JN Mandel, JL Moraine, C Mulley, J Nelson, D Oostra, B Partington, M Ramakers, GJA Ropers, HH Rousseau, F Schwartz, C Steinbach, P Stoll, C Tranebjaerg, L Turner, G Van Bokhoven, H Vianna-Morgante, A Villard, L Warren, ST
Citation: Jp. Fryns et al., 9th international workshop on fragile X syndrome and X-linked mental retardation, AM J MED G, 94(5), 2000, pp. 345-360

Authors: Steinlein, OK Stoodt, J Mulley, J Berkovic, S Scheffer, IE Brodtkorb, E
Citation: Ok. Steinlein et al., Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsy, EPILEPSIA, 41(5), 2000, pp. 529-535

Authors: Merienne, K Jacquot, S Pannetier, S Zeniou, M Bankier, A Gecz, J Mandel, JL Mulley, J Sassone-Corsi, P Hanauer, A
Citation: K. Merienne et al., A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation, NAT GENET, 22(1), 1999, pp. 13-14

Authors: McDermott, MF Aksentijevich, I Galon, J McDermott, EM Ogunkolade, BW Centola, M Mansfield, E Gadina, M Karenko, L Pettersson, T McCarthy, J Frucht, DM Aringer, M Torosyan, Y Teppo, AM Wilson, M Karaarslan, HM Wan, Y Todd, I Wood, G Schlimgen, R Kumarajeewa, TR Cooper, SM Vella, JP Amos, CI Mulley, J Quane, KA Molloy, MG Ranki, A Powell, RJ Hitman, GA O'Shea, JJ Kastner, DL
Citation: Mf. Mcdermott et al., Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes, CELL, 97(1), 1999, pp. 133-144
Risultati: 1-5 |