APA (7th ed.) Citation

AP, R., K, F., L, R., & CP, B. (2021). A de novo missense variant in MED13 in a patient with global developmental delay, marked facial dysmorphism, macroglossia, short stature, and macrocephaly. American journal of medical genetics. Part A, 185(8), 2586. https://doi.org/10.1002/ajmg.a.62238

Chicago Style (17th ed.) Citation

AP, Rogers, Friend K, Rawlings L, and Barnett CP. "A De Novo Missense Variant in MED13 in a Patient with Global Developmental Delay, Marked Facial Dysmorphism, Macroglossia, Short Stature, and Macrocephaly." American Journal of Medical Genetics. Part A 185, no. 8 (2021): 2586. https://doi.org/10.1002/ajmg.a.62238.

MLA (9th ed.) Citation

AP, Rogers, et al. "A De Novo Missense Variant in MED13 in a Patient with Global Developmental Delay, Marked Facial Dysmorphism, Macroglossia, Short Stature, and Macrocephaly." American Journal of Medical Genetics. Part A, vol. 185, no. 8, 2021, p. 2586, https://doi.org/10.1002/ajmg.a.62238.