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Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins.
Jaballah-Gabteni A, Tounsi H, Kabbage M, Hamdi Y, Elouej S, Ben Ayed I, Medhioub M, Mahmoudi M, Dallali H, Yaiche H, Ben Jemii N, Maaloul A, Mezghani N, Abdelhak S, Hamzaoui L, Azzouz M, Boubaker S. Jaballah-Gabteni A, et al. Among authors: maaloul a. J Transl Med. 2019 Jun 27;17(1):212. doi: 10.1186/s12967-019-1961-9. J Transl Med. 2019. PMID: 31248416 Free PMC article.
A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma.
Kabbage M, Ben Aissa-Haj J, Othman H, Jaballah-Gabteni A, Laarayedh S, Elouej S, Medhioub M, Kettiti HT, Khsiba A, Mahmoudi M, BelFekih H, Maaloul A, Touinsi H, Hamzaoui L, Chelbi E, Abdelhak S, Boubaker MS, Azzouz MM. Kabbage M, et al. Among authors: maaloul a. Genes (Basel). 2022 Jul 28;13(8):1355. doi: 10.3390/genes13081355. Genes (Basel). 2022. PMID: 36011265 Free PMC article.
CDH1 Germline Variants in a Tunisian Cohort with Hereditary Diffuse Gastric Carcinoma.
Ben Aissa-Haj J, Kabbage M, Othmen H, Saulnier P, Kettiti HT, Jaballah-Gabteni A, Ferah A, Medhioub M, Khsiba A, Mahmoudi M, Maaloul A, Ben Nasr S, Chelbi E, Abdelhak S, Boubaker MS, Azzouz MM, Rouleau E. Ben Aissa-Haj J, et al. Among authors: maaloul a. Genes (Basel). 2022 Feb 23;13(3):400. doi: 10.3390/genes13030400. Genes (Basel). 2022. PMID: 35327954 Free PMC article.