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Journal of Pediatric Genetics|November 17, 2017
Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the LiteratureMolka Kammoun, Wafa Slimani, Hanene Hannachi, et al.Journal of Assisted Reproduction and Genetics|August 20, 2011
Detection of aneuploidy rate for chromosomes X, Y and 8 by fluorescence in-situ hybridization in spermatozoa from patients with severe non-obstructive oligozoospermiaSoumaya Mougou-Zerelli, Sonia Brahem, Molka Kammoun, et al.La Tunisie Medicale|March 18, 2026
Why publish? Perspectives of North African researchers in the medical fieldMeriem Gaddas, Rym Fakfekh, Rihem Dahmane, et al.Journal of Pediatric Genetics|May 13, 2017
Genomic Microarray in Intellectual Disability: The Usefulness of Existing Systems in the Interpretation of Copy Number VariationHela Ben Khelifa, Najla Soyah, Audrey Labalme, et al.European Journal of Medical Genetics|July 6, 2021
Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian caseKhouloud Rjiba, Najla Soyah, Molka Kammoun, et al.Frontiers in Genetics|February 13, 2023
Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?Rahma Touhami, Hajer Foddha, Eudeline Alix, et al.Journal of Pediatric Genetics|September 13, 2016
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical TraitsHela Ben Khelifa, Molka Kammoun, Hanene Hannachi, et al.International Journal of Fertility & Sterility|June 24, 2018
Subtelomeric Rearrangements in Patients with Recurrent MiscarriageAmani Hajlaoui, Wafa Slimani, Molka Kammoun, et al.Gene|June 25, 2013
Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardationHela Ben Khelifa, Najla Soyah, Inesse Ben-Abdallah-Bouhjar, et al.Molecular Cytogenetics|February 25, 2021
Disorders of sex development in Wolf-Hirschhorn syndrome: a genotype-phenotype correlation and MSX1 as candidate geneKhouloud Rjiba, Hédia Ayech, Olfa Kraiem, et al.Pageof 3