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You searched for: Author/Creator Messaoud, Olfa

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1. A broad survey of DNA sequence data simulation tools. (23rd December 2019)

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

3. A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC26A4 gene. (25th April 2019)

5. 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)

6. Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia. Issue 2 (16th July 2015)

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

8. Further Evidence of Mutational Heterogeneity of the XPC Gene in Tunisian Families: A Spectrum of Private and Ethnic Specific Mutations. (25th July 2013)

9. H syndrome: Clinical, histological and genetic investigation in Tunisian patients. Issue 8 (29th May 2018)

10. High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis. Issue 2 (5th February 2014)