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Kabbage M, Ben Aissa-Haj J, Othman H, Jaballah-Gabteni A, Laarayedh S, Elouej S, Medhioub M, Kettiti HT, Khsiba A, Mahmoudi M, et al. A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma. Genes. 2022; 13(8):1355. https://doi.org/10.3390/genes13081355

Kabbage, Maria, Jihenne Ben Aissa-Haj, Houcemeddine Othman, Amira Jaballah-Gabteni, Sarra Laarayedh, Sahar Elouej, Mouna Medhioub, Haifa Tounsi Kettiti, Amal Khsiba, Moufida Mahmoudi, and et al. 2022. "A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma" Genes 13, no. 8: 1355. https://doi.org/10.3390/genes13081355

Kabbage, M., Ben Aissa-Haj, J., Othman, H., Jaballah-Gabteni, A., Laarayedh, S., Elouej, S., Medhioub, M., Kettiti, H. T., Khsiba, A., Mahmoudi, M., BelFekih, H., Maaloul, A., Touinsi, H., Hamzaoui, L., Chelbi, E., Abdelhak, S., Boubaker, M. S., & Azzouz, M. M. (2022). A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma. Genes, 13(8), 1355. https://doi.org/10.3390/genes13081355