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Results: 1-2 |
Results: 2
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications forthe disease
Authors: Villard, L Levy, N Xiang, FQ Kpebe, A Labelle, V Chevillard, C Zhang, ZP Schwartz, CE Tardieu, M Chelly, J Anvret, M Fontes, M
Citation: L. Villard et al., Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications forthe disease, J MED GENET, 38(7), 2001, pp. 435-442
Two affected boys in a Rett syndrome family - Clinical and molecular findings
Authors: Villard, L Kpebe, A Cardoso, C Chelly, J Tardieu, M Fontes, M
Citation: L. Villard et al., Two affected boys in a Rett syndrome family - Clinical and molecular findings, NEUROLOGY, 55(8), 2000, pp. 1188-1193
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