Farncombe, K. M., Thain, E., Barnett-Tapia, C., Sadeghian, H., & Kim, R. H. (2022). LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis. BMC Medical Genomics, 15(1), 1. https://doi.org/10.1186/s12920-022-01304-x
Chicago Style (17th ed.) CitationFarncombe, Kirsten M., Emily Thain, Carolina Barnett-Tapia, Hamid Sadeghian, and Raymond H. Kim. "LZTR1 Molecular Genetic Overlap with Clinical Implications for Noonan Syndrome and Schwannomatosis." BMC Medical Genomics 15, no. 1 (2022): 1. https://doi.org/10.1186/s12920-022-01304-x.
MLA (9th ed.) CitationFarncombe, Kirsten M., et al. "LZTR1 Molecular Genetic Overlap with Clinical Implications for Noonan Syndrome and Schwannomatosis." BMC Medical Genomics, vol. 15, no. 1, 2022, p. 1, https://doi.org/10.1186/s12920-022-01304-x.