APA (7th ed.) Citation

PS, O., A, U., KT, S. P., S, V., J, S., K, V. S., & SJ, P. (2026). Tetralogy of Fallot and craniosynostosis - differential manifestation in a familial case of CHDED syndrome caused by novel pathogenic PRKD1 variant. Journal of human genetics, 71(3), 177. https://doi.org/10.1038/s10038-025-01415-0

Chicago Style (17th ed.) Citation

PS, Oza, Uttarilli A, Shreya Parthasarathi KT, Viswanathan S, Sharma J, V S. K, and Patil SJ. "Tetralogy of Fallot and Craniosynostosis - Differential Manifestation in a Familial Case of CHDED Syndrome Caused by Novel Pathogenic PRKD1 Variant." Journal of Human Genetics 71, no. 3 (2026): 177. https://doi.org/10.1038/s10038-025-01415-0.

MLA (9th ed.) Citation

PS, Oza, et al. "Tetralogy of Fallot and Craniosynostosis - Differential Manifestation in a Familial Case of CHDED Syndrome Caused by Novel Pathogenic PRKD1 Variant." Journal of Human Genetics, vol. 71, no. 3, 2026, p. 177, https://doi.org/10.1038/s10038-025-01415-0.