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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
Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A
Authors: Bernard, R Labelle, V Negre, P Tardieu, S Azulay, JP Malzac, P Mattei, JF Leguern, E Philip, N Levy, N
Citation: R. Bernard et al., Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A, EUR J HUM G, 8(3), 2000, pp. 229-235
Risultati: 1-2 |