Search Results - Raclin, V

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    De novo deletions in spinal muscular atrophy: implications for genetic counselling.

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

    Published 1997
    Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

    Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes. by Melki, J, Abdelhak, S, Burlet, P, Raclin, V, Kaplan, J, Spiegel, R, Gilgenkrantz, S, Philip, N, Chauvet, M L, Dumez, Y

    Published 1992
    Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy by Amiel, J., Raclin, V., Jouannic, J., Morichon, N., Hoffman-Radvanyi, H., Dommergues, M., Feingold, J., Munnich, A., Bonnefont, J.

    Published 2001
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  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. by Bürglen, L, Amiel, J, Viollet, L, Lefebvre, S, Burlet, P, Clermont, O, Raclin, V, Landrieu, P, Verloes, A, Munnich, A, Melki, J

    Published 1996
    Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: