APA (7th ed.) Citation

Lee, C., Chang, Y., Chuang, C., Chiu, H., Tu, Y., Lo, Y., . . . Lin, S. (2026). From Array-CGH to Whole-Genome Sequencing: A 29-Year Diagnostic Journey Culminating in the Identification of a De Novo ABCC9 Variant Consistent with Cantú Syndrome. Diagnostics (2075-4418), 16(14), 2204. https://doi.org/10.3390/diagnostics16142204

Chicago Style (17th ed.) Citation

Lee, Chung-Lin, Ya-Hui Chang, Chih-Kuang Chuang, Huei-Ching Chiu, Yuan-Rong Tu, Yun-Ting Lo, Jun-Yi Wu, Hsiang-Yu Lin, and Shuan-Pei Lin. "From Array-CGH to Whole-Genome Sequencing: A 29-Year Diagnostic Journey Culminating in the Identification of a De Novo ABCC9 Variant Consistent with Cantú Syndrome." Diagnostics (2075-4418) 16, no. 14 (2026): 2204. https://doi.org/10.3390/diagnostics16142204.

MLA (9th ed.) Citation

Lee, Chung-Lin, et al. "From Array-CGH to Whole-Genome Sequencing: A 29-Year Diagnostic Journey Culminating in the Identification of a De Novo ABCC9 Variant Consistent with Cantú Syndrome." Diagnostics (2075-4418), vol. 16, no. 14, 2026, p. 2204, https://doi.org/10.3390/diagnostics16142204.