Search Results - Elgaied-Boulila, Amel

  • Showing 1 - 5 results of 5
Refine Results
  1. 1
    Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

    Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness by Masmoudi, Saber, Antonarakis, Stylianos E., Schwede, Torsten, Ghorbel, Abdel Monem, Gratri, M'hamed, Pappasavas, Marie-Pierre, Drira, Mohamed, Elgaied-Boulila, Amel, Wattenhofer, Marie, Rossier, Colette, Scott, Hamish S., Ayadi, Hammadi, Guipponi, Michel

    Published in Human mutation
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates

    Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates by Ben Arab, Saïda, Hmani, Mounira, Denoyelle, Françoise, Boulila-Elgaied, Amel, Chardenoux, Sebastien, Hachicha, Slah, Petit, Christine, Ayadi, Hammadi

    Published in Clinical genetics
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

    Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE by MASMOUDI, SABER, ELGAIED-BOULILA, AMEL, KASSAB, ILYES, ARAB, SAIDA BEN, BLANCHARD, STEPHANE, BOUZOUITA, JA-EL, DRIRA, MOHAMED, KASSAB, AICHA, HACHICHA, SLAH, PETIT, CHRISTINE, AYADI, HAMMADI

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation

    Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation by Masmoudi, Saber, Charfedine, Ilhem, Hmani, Mounira, Grati, M'hamed, Ghorbel, Abdel Monem, Elgaied-Boulila, Amel, Drira, Mohamed, Hardelin, Jean-Pierre, Ayadi, Hammadi

    Get full text
    Article
    Save to List
    Saved in:
  5. 5
    Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation

    Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation by Masmoudi, Saber, Charfedine, Ilhem, Hmani, Mounira, Grati, M'hamed, Ghorbel, Abdel Monem, Elgaied-Boulila, Amel, Drira, Mohamed, Hardelin, Jean-Pierre, Ayadi, Hammadi

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

Search Tools: