Search Results - Snoeckx, R.L.

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    A genotype-phenotype correlation for GJB2 (connexin 26) deafness

    A genotype-phenotype correlation for GJB2 (connexin 26) deafness by Cryns, K, Orzan, E, Murgia, A, Huygen, P L M, Moreno, F, del Castillo, I, Parker Chamberlin, G, Azaiez, H, Prasad, S, Cucci, R A, Leonardi, E, Snoeckx, R L, Govaerts, P J, Van de Heyning, P H, Van de Heyning, C M, Smith, R J H, Van Camp, G

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

    A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3 by Snoeckx, R L, Kremer, H, Ensink, R J H, Flothmann, K, de Brouwer, A, Smith, R J H, Cremers, C W R J, Van Camp, G

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13

    A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13 by Ensink, R.J.H., Huygen, P.L.M., Snoeckx, R.L., Caethoven, G., Van Camp, G., Cremers, C.W.R.J.

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: