NM, E., ML, E., HM, F., OM, E., M, N., AM, M., & CA, T. (2026). Molecular analysis of foveoschisis in females reveals a novel case of segmental uniparental disomy in X-linked retinoschisis. Documenta ophthalmologica. Advances in ophthalmology, 152(2), 145. https://doi.org/10.1007/s10633-025-10053-y
Chicago Style (17th ed.) CitationNM, Elbagoury, Essawi ML, Fathy HM, Eid OM, Nabih M, Mohamed AM, and Tawfik CA. "Molecular Analysis of Foveoschisis in Females Reveals a Novel Case of Segmental Uniparental Disomy in X-linked Retinoschisis." Documenta Ophthalmologica. Advances in Ophthalmology 152, no. 2 (2026): 145. https://doi.org/10.1007/s10633-025-10053-y.
MLA (9th ed.) CitationNM, Elbagoury, et al. "Molecular Analysis of Foveoschisis in Females Reveals a Novel Case of Segmental Uniparental Disomy in X-linked Retinoschisis." Documenta Ophthalmologica. Advances in Ophthalmology, vol. 152, no. 2, 2026, p. 145, https://doi.org/10.1007/s10633-025-10053-y.