APA (7th ed.) Citation

E, B., E, G., G, M., E, L., S, L., M, Y., . . . S, S. (2011). Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression. Human molecular genetics, 20(18), 3632. https://doi.org/10.1093/hmg/ddr283

Chicago Style (17th ed.) Citation

E, Ben-David, Granot-Hershkovitz E, Monderer-Rothkoff G, Lerer E, Levi S, Yaari M, Ebstein RP, Yirmiya N, and Shifman S. "Identification of a Functional Rare Variant in Autism Using Genome-wide Screen for Monoallelic Expression." Human Molecular Genetics 20, no. 18 (2011): 3632. https://doi.org/10.1093/hmg/ddr283.

MLA (9th ed.) Citation

E, Ben-David, et al. "Identification of a Functional Rare Variant in Autism Using Genome-wide Screen for Monoallelic Expression." Human Molecular Genetics, vol. 20, no. 18, 2011, p. 3632, https://doi.org/10.1093/hmg/ddr283.