APA (7th ed.) Citation

Moriura, Y., Nishio, Y., Ichimura, S., Noda, H., Tanahashi, Y., Yamamoto, H., . . . Ogi, T. (2025). De novo CDKN1C variant in Beckwith–Wiedermann spectrum with atypical complications. Human genome variation, 12(1), 9-3. https://doi.org/10.1038/s41439-025-00316-0

Chicago Style (17th ed.) Citation

Moriura, Yuri, et al. "De Novo CDKN1C Variant in Beckwith–Wiedermann Spectrum with Atypical Complications." Human Genome Variation 12, no. 1 (2025): 9-3. https://doi.org/10.1038/s41439-025-00316-0.

MLA (9th ed.) Citation

Moriura, Yuri, et al. "De Novo CDKN1C Variant in Beckwith–Wiedermann Spectrum with Atypical Complications." Human Genome Variation, vol. 12, no. 1, 2025, pp. 9-3, https://doi.org/10.1038/s41439-025-00316-0.