I, S., M, J., & A, M. (2026). Best practices in demographic data collection for equity, diversity, and inclusion in rare disease research: A systematic review. Genetics in medicine : official journal of the American College of Medical Genetics, 28(7), 102592. https://doi.org/10.1016/j.gim.2026.102592
Παραπομπή σε μορφή Chicago (17η εκδ.)I, Sinan, Johnston M, και Marwaha A. "Best Practices in Demographic Data Collection for Equity, Diversity, and Inclusion in Rare Disease Research: A Systematic Review." Genetics in Medicine : Official Journal of the American College of Medical Genetics 28, no. 7 (2026): 102592. https://doi.org/10.1016/j.gim.2026.102592.
Παραπομπή σε μορφή MLA (9th εκδ.)I, Sinan, et al. "Best Practices in Demographic Data Collection for Equity, Diversity, and Inclusion in Rare Disease Research: A Systematic Review." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 28, no. 7, 2026, p. 102592, https://doi.org/10.1016/j.gim.2026.102592.