Hela Sassi

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

R. M’rad, S. Hannachi, Hela Sassi, 2022, BMC medical genomics.

JAK2 p.(V617F) mutation in Tunisian myeloproliferative neoplasms and its genotype-phenotype correlation

S. Menif, Hela Sassi, Safa Ben Ammar, 2021, The Pan African medical journal.