He, G., Maslen, C. L., Chen, H., Hou, H., Bai, X., Wang, X., . . . Yang, Q. (2022). Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications. Clinical genetics, 102(5), 391-403. https://doi.org/10.1111/cge.14201
Chicago Style (17th ed.) CitationHe, Guo‐Wei, et al. "Identification of Novel Rare Copy Number Variants Associated with Sporadic Tetralogy of Fallot and Clinical Implications." Clinical Genetics 102, no. 5 (2022): 391-403. https://doi.org/10.1111/cge.14201.
MLA (9th ed.) CitationHe, Guo‐Wei, et al. "Identification of Novel Rare Copy Number Variants Associated with Sporadic Tetralogy of Fallot and Clinical Implications." Clinical Genetics, vol. 102, no. 5, 2022, pp. 391-403, https://doi.org/10.1111/cge.14201.