APA (7th ed.) Citation

Touhami, R., Foddha, H., Alix, E., Jalloul, A., Mougou-Zerelli, S., Saad, A., . . . Khelil, A. H. (2023). Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient’s phenotype? R. Frontiers in genetics, 13, 1. https://doi.org/10.3389/fgene.2022.1061539

Chicago Style (17th ed.) Citation

Touhami, Rahma, Hajer Foddha, Eudeline Alix, Afef Jalloul, Soumaya Mougou-Zerelli, Ali Saad, Damien Sanlaville, and Amel Haj Khelil. "Case Report: 7p22.3 Deletion and 8q24.3 Duplication in a Patient with Epilepsy and Psychomotor Delay-Does Both Possibly Act to Modulate a Candidate Gene Region for the Patient’s Phenotype? R." Frontiers in Genetics 13 (2023): 1. https://doi.org/10.3389/fgene.2022.1061539.

MLA (9th ed.) Citation

Touhami, Rahma, et al. "Case Report: 7p22.3 Deletion and 8q24.3 Duplication in a Patient with Epilepsy and Psychomotor Delay-Does Both Possibly Act to Modulate a Candidate Gene Region for the Patient’s Phenotype? R." Frontiers in Genetics, vol. 13, 2023, p. 1, https://doi.org/10.3389/fgene.2022.1061539.