Publications

  1. Amouri A, Talmoudi F, Messaoud O, d’Enghien CD, Rekaya MB, Allegui I, et al. High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis. Mol Genet Genomic Med. mars 2014;2(2):160‑5.
  2. Bouchlaka C, Abdelhak S, Amouri A, Ben Abid H, Hadiji S, Frikha M, et al. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations. J Hum Genet. 2003;48(7):352‑61.
  3. Talmoudi F, Kammoun L, Benhalim N, Torjemane L, Ouederni M, Aissaoui L, et al. Cytogenetic Assessment of Fanconi Anemia in Children With Aplastic Anemia in Tunisia: J Pediatr Hematol Oncol. oct 2013;35(7):547‑50.
  4. Kassar O, Mseddi S, Khanfir A, Slimi L, Bellaaj H, Mdhaffar M, et al. [Fanconi anemia with precocious and inaugural oncologic events]. Tunis Med. févr 2009;87(2):167‑8.
  5. Hadiji Mseddi S, Kammoun L, Bellaaj H, Ben Youssef Y, Aissaoui L, Torjemane L, et al. Création et rapport du registre tunisien de l’anémie de Fanconi (TFAR). Arch Pédiatrie. 1 mai 2012;19(5):467‑75.
  6. Talmoudi F, Kilani O, Ayed W, Ben Halim N, Mellouli F, Torjmane L, et al. Differentiation of Fanconi anemia and aplastic anemia using mitomycin C test in Tunisia. C R Biol. janv 2013;336(1):29‑33.
  7. Frikha M, Mseddi S, Elloumi M, Bouaziz M, Khanfir A, Mnif J, et al. La maladie de Fanconi: étude de 43 cas dans le sud tunisien. Arch Pédiatrie. nov 1998;5(11):1200‑5.