B. Dakhlaoui

Prenatal diagnosis of cystic fibrosis: 10-years experience.

F. Zouari, H. Siala, T. Messaoud, 2015, Pathologie-biologie.

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 between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients

H. Siala, S. Fredj, F. Ouali, 2013, Molecular Biology Reports.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia

H. Siala, T. Messaoud, S. Fredj, 2013, Clinical chemistry and laboratory medicine.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia

H. Siala, T. Messaoud, S. Fredj, 2013, Clinical chemistry and laboratory medicine.

Setup of a Protocol of Molecular Diagnosis of β‐Thalassemia Mutations in Tunisia using Denaturing High‐Performance Liquid Chromatography (DHPLC)

H. Siala, T. Messaoud, S. Hadj Fredj, 2016, Journal of clinical laboratory analysis.

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients

H. Siala, S. Fredj, F. Ouali, 2013, Molecular Biology Reports.