Pierre Bouche

SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease.

J. Melki, A. Brice, J. Pouget, 1997, Journal of medical genetics.

Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Y. Agid, A. Brice, N. Birouk, 1996, American journal of human genetics.

Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.

Y. Agid, A. Brice, G. Stevanin, 1992, Journal of medical genetics.

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases.

Y. Agid, A. Brice, N. Birouk, 1997, Brain : a journal of neurology.