APA (7th ed.) Citation

Nardello, R., Antona, V., Mangano, G. D., Salpietro, V., Mangano, S., & Fontana, A. (2021). A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes. BMC Medical Genomics, 14(1), 1. https://doi.org/10.1186/s12920-021-00934-x

Chicago Style (17th ed.) Citation

Nardello, Rosaria, Vincenzo Antona, Giuseppe Donato Mangano, Vincenzo Salpietro, Salvatore Mangano, and Antonina Fontana. "A Paradigmatic Autistic Phenotype Associated with Loss of PCDH11Y and NLGN4Y Genes." BMC Medical Genomics 14, no. 1 (2021): 1. https://doi.org/10.1186/s12920-021-00934-x.

MLA (9th ed.) Citation

Nardello, Rosaria, et al. "A Paradigmatic Autistic Phenotype Associated with Loss of PCDH11Y and NLGN4Y Genes." BMC Medical Genomics, vol. 14, no. 1, 2021, p. 1, https://doi.org/10.1186/s12920-021-00934-x.