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Results: 1-9 |
Results: 9
Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patients
Authors: Van Buggenhout, GJCM van Ravenswaaij-Arts, C Mieloo, H Syrrou, M Hamel, B Brunner, H Fryns, JP
Citation: Gjcm. Van Buggenhout et al., Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patients, ANN GENET, 44(2), 2001, pp. 89-92
Pharmacokinetics of enoxacin and its oxometabolite after multiple oral dosing and penetration into prostatic tissue
Authors: Hamel, B Mottet, N Audran, M Costa, P Bressolle, F
Citation: B. Hamel et al., Pharmacokinetics of enoxacin and its oxometabolite after multiple oral dosing and penetration into prostatic tissue, J ANTIMICRO, 46(6), 2000, pp. 993-996
Cosegregation of T108A Elk-1 with mental retardation
Authors: Schroer, A Scheer, MP Zacharias, S Schneider, S Ropers, HH Nothwang, HG Chelly, J Hamel, B Fryns, JP Shaw, P Moraine, C
Citation: A. Schroer et al., Cosegregation of T108A Elk-1 with mental retardation, AM J MED G, 95(4), 2000, pp. 404-405
9th international workshop on fragile X syndrome and X-linked mental retardation
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
Diffusion of enoxacin and its oxo-metabolite into human epididymal tissue
Authors: Hamel, B Mottet, N Audran, M Costa, P Bressolle, F
Citation: B. Hamel et al., Diffusion of enoxacin and its oxo-metabolite into human epididymal tissue, EUR J CL PH, 56(8), 2000, pp. 597-598
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
Authors: Carrie, A Jun, L Bienvenu, T Vinet, MC McDonell, N Couvert, P Zemni, R Cardona, A Van Buggenhout, G Frints, S Hamel, B Moraine, C Ropers, HH Strom, T Howell, GR Whittaker, A Ross, MT Kahn, A Fryns, JP Beldjord, C Marynen, P Chelly, J
Citation: A. Carrie et al., A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation, NAT GENET, 23(1), 1999, pp. 25-31
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations
Authors: Nelen, MR Kremer, H Konings, IBM Schoute, F van Essen, AJ Koch, R Woods, CG Fryns, JP Hamel, B Hoefsloot, LH Peeters, EAJ Padberg, GW
Citation: Mr. Nelen et al., Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations, EUR J HUM G, 7(3), 1999, pp. 267-273
X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: The European XLMR Consortium
Authors: des Portes, V Beldjord, C Chelly, J Hamel, B Kremer, H Smits, A van Bokhoven, H Ropers, HH Claes, S Fryns, JP Ronce, N Gendrot, C Toutain, A Raynaud, M Moraine, C
Citation: V. Des Portes et al., X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: The European XLMR Consortium, AM J MED G, 85(3), 1999, pp. 263-265
The first nuclear-encoded complex I mutation in a patient with leigh syndrome
Authors: Loeffen, J Smeitink, A Triepels, R Smeets, R Schuelke, M Sengers, R Trijbels, F Hamel, B Mullaart, R van den Heuvel, L
Citation: J. Loeffen et al., The first nuclear-encoded complex I mutation in a patient with leigh syndrome, AM J HU GEN, 63(6), 1998, pp. 1598-1608
Risultati: 1-9 |