APA (7th ed.) Citation

J, C., K, C., F, L., O, Q., S, C., C, D., . . . G, N. (2022). Deep intronic NIPBL de novo mutations and differential diagnoses revealed by whole genome and RNA sequencing in Cornelia de Lange syndrome patients. Human mutation, 43(12), 1882. https://doi.org/10.1002/humu.24438

Chicago Style (17th ed.) Citation

J, Coursimault, et al. "Deep Intronic NIPBL De Novo Mutations and Differential Diagnoses Revealed by Whole Genome and RNA Sequencing in Cornelia De Lange Syndrome Patients." Human Mutation 43, no. 12 (2022): 1882. https://doi.org/10.1002/humu.24438.

MLA (9th ed.) Citation

J, Coursimault, et al. "Deep Intronic NIPBL De Novo Mutations and Differential Diagnoses Revealed by Whole Genome and RNA Sequencing in Cornelia De Lange Syndrome Patients." Human Mutation, vol. 43, no. 12, 2022, p. 1882, https://doi.org/10.1002/humu.24438.