E, W., N, H., S, A., IR, E., & M, B. (2024). ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. Clinical genetics, 105(5), 470. https://doi.org/10.1111/cge.14506
Chicago Style (17th ed.) CitationE, Woods, Holmes N, Albaba S, Evans IR, and Balasubramanian M. "ASXL3-related Disorder: Molecular Phenotyping and Comprehensive Review Providing Insights into Disease Mechanism." Clinical Genetics 105, no. 5 (2024): 470. https://doi.org/10.1111/cge.14506.
MLA (9th ed.) CitationE, Woods, et al. "ASXL3-related Disorder: Molecular Phenotyping and Comprehensive Review Providing Insights into Disease Mechanism." Clinical Genetics, vol. 105, no. 5, 2024, p. 470, https://doi.org/10.1111/cge.14506.