Maternally inherited duplication of the possible imprinted 14q31 region

Por Mignon-Ravix, C., Mugneret, F., Stavropoulou, C., Depetris, D., Van Kien, P. K., Mattei, M.
Publicado em 2001

Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations

Por Luciani, J, de Mas, P, Depetris, D, Mignon-Ravix, C, Bottani, A, Prieur, M, Jonveaux, P, Philippe, A, Bourrouillou, G, de Martinville, B, Delobel, B, Vallee, L, Croquette, M, Mattei, M
Publicado em 2003