All Stories

  1. Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits

    Article • Journal of Pediatric Genetics, October 2015, Thieme Publishing Group

    Dr Hela BEN KHELIFA

  2. Xp22.3 interstitial deletion: A recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation

    Article • Gene, September 2013, Elsevier

    Dr Hela BEN KHELIFA

  3. Phenotype and Micro-array characterization of duplication 11q22.1-q25 and review of the literature

    Article • Gene, April 2013, Elsevier

    Dr Hela BEN KHELIFA