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You searched for: Author/Creator Naouali, Chokri

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1. A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy. (3rd May 2014)

2. Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome. Issue 7 (23rd May 2019)

3. Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients. (26th October 2016)

4. Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus. Issue 6 (18th June 2019)

5. On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations. (2nd January 2018)

6. Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis. Issue 2 (February 2018)