M, B., AJM, D., S, A., R, R., TM, Y., H, C., . . . T, K. (2021). Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. European journal of human genetics : EJHG, 29(4), 625. https://doi.org/10.1038/s41431-020-00769-7
Chicago Style (17th ed.) CitationM, Balasubramanian, et al. "Comprehensive Study of 28 Individuals with SIN3A-related Disorder Underscoring the Associated Mild Cognitive and Distinctive Facial Phenotype." European Journal of Human Genetics : EJHG 29, no. 4 (2021): 625. https://doi.org/10.1038/s41431-020-00769-7.
MLA (9th ed.) CitationM, Balasubramanian, et al. "Comprehensive Study of 28 Individuals with SIN3A-related Disorder Underscoring the Associated Mild Cognitive and Distinctive Facial Phenotype." European Journal of Human Genetics : EJHG, vol. 29, no. 4, 2021, p. 625, https://doi.org/10.1038/s41431-020-00769-7.