APA (7th ed.) Citation

Ganesh, S., Vemula, A., Bhattacharjee, S., Mathew, K., Ithal, D., Navin, K., . . . Kannan, R. (2022). Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes. Scientific Reports, 12(1), 1. https://doi.org/10.1038/s41598-022-25664-7

Chicago Style (17th ed.) Citation

Ganesh, Suhas, et al. "Whole Exome Sequencing in Dense Families Suggests Genetic Pleiotropy Amongst Mendelian and Complex Neuropsychiatric Syndromes." Scientific Reports 12, no. 1 (2022): 1. https://doi.org/10.1038/s41598-022-25664-7.

MLA (9th ed.) Citation

Ganesh, Suhas, et al. "Whole Exome Sequencing in Dense Families Suggests Genetic Pleiotropy Amongst Mendelian and Complex Neuropsychiatric Syndromes." Scientific Reports, vol. 12, no. 1, 2022, p. 1, https://doi.org/10.1038/s41598-022-25664-7.