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• Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

  Mahmoud T, Sahli C, Hadj Fredj S, Amri Y, Othmani R, Mohamed GS, Zein E, Messaoud T. Mahmoud T, et al. Mol Genet Genomic Med. 2022 Oct;10(10):e2048. doi: 10.1002/mgg3.2048. Epub 2022 Sep 15. Mol Genet Genomic Med. 2022. PMID: 36106931 Free PMC article.
• Molecular and physical arrangements of human DNA in HRAS1-selected, chromosome-mediated transfectants.

  Porteous DJ, Morten JE, Cranston G, Fletcher JM, Mitchell A, van Heyningen V, Fantes JA, Boyd PA, Hastie ND. Porteous DJ, et al. Mol Cell Biol. 1986 Jun;6(6):2223-32. doi: 10.1128/mcb.6.6.2223-2232.1986. Mol Cell Biol. 1986. PMID: 3785194 Free PMC article.
• Mediterranean types of beta-thalassemia in the German population.

  Laig M, Pape M, Hundrieser J, Flatz G. Laig M, et al. Hum Genet. 1990 Jun;85(1):135-7. doi: 10.1007/BF00276342. Hum Genet. 1990. PMID: 2162807
• The peculiar spectrum of beta-thalassemia genes in Tunisia.

  Chibani J, Vidaud M, Duquesnoy P, Bergé-Lefranc JL, Pirastu M, Ellouze F, Rosa J, Goossens M. Chibani J, et al. Hum Genet. 1988 Feb;78(2):190-2. doi: 10.1007/BF00278196. Hum Genet. 1988. PMID: 3422218
• Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variants.

  Girodon E, Ghanem N, Vidaud M, Riou J, Martin J, Galactéros F, Goossens M. Girodon E, et al. Ann Hematol. 1992 Oct;65(4):188-92. doi: 10.1007/BF01703113. Ann Hematol. 1992. PMID: 1420507