Resultados de procura - Raclin, V

  • Mostrando 1 - 4 Resultados de 4
Limitar resultados
  1. 1
    De novo deletions in spinal muscular atrophy: implications for genetic counselling.

    De novo deletions in spinal muscular atrophy: implications for genetic counselling. por Raclin, V, Veber, P S, Bürglen, L, Munnich, A, Melki, J

    Publicado 1997
    Ligazón do recurso Ligazón do recurso
    Text
    Engadir a favoritos
    Gardado en:
  2. 2
    Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

    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 1992
    Ligazón do recurso Ligazón do recurso
    Text
    Engadir a favoritos
    Gardado en:
  3. 3
    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

    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 2001
    Ligazón do recurso Ligazón do recurso Ligazón do recurso
    Text
    Engadir a favoritos
    Gardado en:
  4. 4
    Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.

    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 1996
    Ligazón do recurso Ligazón do recurso
    Text
    Engadir a favoritos
    Gardado en:

Ferramentas de procura: