S. Oueslati

New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient

H. Siala, T. Messaoud, S. Fredj, 2013, Journal of Genetics.

Association of TGFB1 -509C/T polymorphism gene with clinical variability in cystic fibrosis patients: A case-control study.

H. Siala, T. Messaoud, S. Fredj, 2015, Pathologie-biologie.

Association of Vitamin D Receptor Gene Polymorphisms With the Evolution of MODY Diabetes: Study in Tunisian Patients

A. Bibi, S. Oueslati, E. Haouat, 2021, Biological research for nursing.

Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation.

H. Siala, T. Messaoud, S. Fredj, 2015, Acta physiologica Hungarica.

Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients

S. Barsaoui, L. Boughamoura, K. Boussetta, 2016, Journal of Genetics.

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations

H. Jamoussi, S. Hadj-Fredj, T. Messaoud, 2021, Molecular Biology Reports.

New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient

H. Siala, T. Messaoud, S. Fredj, 2013, Journal of Genetics.