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Results: 1-6 |
Results: 6

Authors: Tuncbilek, E Alikasifoglu, M Aktas, D Duman, F Yanik, H Anar, B Oostra, B Willemsen, R
Citation: E. Tuncbilek et al., Screening for the fragile X syndrome among mentally retarded males by hairroot analysis, AM J MED G, 95(2), 2000, pp. 105-107

Authors: Tamanini, F Bontekoe, C Bakker, CE van Unen, L Anar, B Willemsen, R Yoshida, M Galjaard, H Oostra, BA Hoogeveen, AT
Citation: F. Tamanini et al., Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations, HUM MOL GEN, 8(5), 1999, pp. 863-869

Authors: Boduroglu, K Alikasifoglu, M Anar, B Tuncbilek, E
Citation: K. Boduroglu et al., Association of the 677C -> T mutation on the methylenetetrahydrofolate reductase gene in turkish patients with neural tube defects, J CHILD NEU, 14(3), 1999, pp. 159-161

Authors: Alikasifoglu, M Topaloglu, H Tuncbilek, E Ceviz, M Anar, B Demir, E Ozme, S
Citation: M. Alikasifoglu et al., Clinical and genetic correlate in childhood onset Friedreich ataxia, NEUROPEDIAT, 30(2), 1999, pp. 72-76

Authors: Tuncbilek, E Alikasifoglu, M Boduroglu, K Aktas, D Anar, B
Citation: E. Tuncbilek et al., Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology, AM J MED G, 84(3), 1999, pp. 202-203

Authors: Willemsen, R Anar, B Otero, YD de Vries, BBA Hilhorst-Hofstee, Y Smits, A van Looveren, E Willems, PJ Galjaard, H Oostra, BA
Citation: R. Willemsen et al., Noninvasive test for fragile X syndrome, using hair root analysis, AM J HU GEN, 65(1), 1999, pp. 98-103
Risultati: 1-6 |