Lantieri, F., Gimelli, S., Viaggi, C., Stathaki, E., Malacarne, M., Santamaria, G., . . . Ceccherini, I. (2019). Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease. Orphanet journal of rare diseases, 14(1), 270-16. https://doi.org/10.1186/s13023-019-1205-3
Chicago Style (17th ed.) CitationLantieri, Francesca, et al. "Copy Number Variations in Candidate Genomic Regions Confirm Genetic Heterogeneity and Parental Bias in Hirschsprung Disease." Orphanet Journal of Rare Diseases 14, no. 1 (2019): 270-16. https://doi.org/10.1186/s13023-019-1205-3.
MLA (9th ed.) CitationLantieri, Francesca, et al. "Copy Number Variations in Candidate Genomic Regions Confirm Genetic Heterogeneity and Parental Bias in Hirschsprung Disease." Orphanet Journal of Rare Diseases, vol. 14, no. 1, 2019, pp. 270-16, https://doi.org/10.1186/s13023-019-1205-3.