Arlette Kpebe

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome withoutMECP2 mutation: implications for the disease

N. Lévy, J. Chelly, M. Anvret, 2001, Journal of medical genetics.

Two affected boys in a Rett syndrome family

J. Chelly, L. Villard, M. Tardieu, 2000, Neurology.

Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling

L. Villard, A. Moncla, C. Missirian, 2002, European Journal of Human Genetics.