Cite
Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1.
MLA
Uludağ Alkaya, Dilek, et al. “Expanding the Clinical Phenotype of RASopathies in 38 Turkish Patients, Including the Rare LZTR1, RAF1, RIT1 Variants, and Large Deletion in NF1.” American Journal of Medical Genetics. Part A, vol. 185, no. 12, Dec. 2021, pp. 3623–33. EBSCOhost, https://doi.org/10.1002/ajmg.a.62410.
APA
Uludağ Alkaya, D., Lissewski, C., Yeşil, G., Zenker, M., & Tüysüz, B. (2021). Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1. American Journal of Medical Genetics. Part A, 185(12), 3623–3633. https://doi.org/10.1002/ajmg.a.62410
Chicago
Uludağ Alkaya, Dilek, Christina Lissewski, Gözde Yeşil, Martin Zenker, and Beyhan Tüysüz. 2021. “Expanding the Clinical Phenotype of RASopathies in 38 Turkish Patients, Including the Rare LZTR1, RAF1, RIT1 Variants, and Large Deletion in NF1.” American Journal of Medical Genetics. Part A 185 (12): 3623–33. doi:10.1002/ajmg.a.62410.