Weiss, K., Lazar, H. P., Kurolap, A., Martinez, A. F., Paperna, T., Cohen, L., . . . Lachlan, K. (2020). The CHD4-related syndrome: A comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis. Genetics in medicine, 22(2), 389-397. https://doi.org/10.1038/s41436-019-0612-0
Chicago Style (17th ed.) CitationWeiss, Karin, et al. "The CHD4-related Syndrome: A Comprehensive Investigation of the Clinical Spectrum, Genotype–phenotype Correlations, and Molecular Basis." Genetics in Medicine 22, no. 2 (2020): 389-397. https://doi.org/10.1038/s41436-019-0612-0.
MLA (9th ed.) CitationWeiss, Karin, et al. "The CHD4-related Syndrome: A Comprehensive Investigation of the Clinical Spectrum, Genotype–phenotype Correlations, and Molecular Basis." Genetics in Medicine, vol. 22, no. 2, 2020, pp. 389-397, https://doi.org/10.1038/s41436-019-0612-0.