De novo deletions in spinal muscular atrophy: implications for genetic counselling.

Por Raclin, V, Veber, P S, Bürglen, L, Munnich, A, Melki, J
Publicado em 1997

Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

Por Melki, J, Abdelhak, S, Burlet, P, Raclin, V, Kaplan, J, Spiegel, R, Gilgenkrantz, S, Philip, N, Chauvet, M L, Dumez, Y
Publicado em 1992

Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

Por Amiel, J., Raclin, V., Jouannic, J., Morichon, N., Hoffman-Radvanyi, H., Dommergues, M., Feingold, J., Munnich, A., Bonnefont, J.
Publicado em 2001

Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.

Por Bürglen, L, Amiel, J, Viollet, L, Lefebvre, S, Burlet, P, Clermont, O, Raclin, V, Landrieu, P, Verloes, A, Munnich, A, Melki, J
Publicado em 1996