APA (7th ed.) Citation

SV, M., SD, K., RH, S., E, V., & JA, M. (2019). Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. Molecular genetics & genomic medicine, 7(2), e00501. https://doi.org/10.1002/mgg3.501

Chicago Style (17th ed.) Citation

SV, Mullegama, Klein SD, Signer RH, Vilain E, and Martinez-Agosto JA. "Mutations in STAG2 Cause an X-linked Cohesinopathy Associated with Undergrowth, Developmental Delay, and Dysmorphia: Expanding the Phenotype in Males." Molecular Genetics & Genomic Medicine 7, no. 2 (2019): e00501. https://doi.org/10.1002/mgg3.501.

MLA (9th ed.) Citation

SV, Mullegama, et al. "Mutations in STAG2 Cause an X-linked Cohesinopathy Associated with Undergrowth, Developmental Delay, and Dysmorphia: Expanding the Phenotype in Males." Molecular Genetics & Genomic Medicine, vol. 7, no. 2, 2019, p. e00501, https://doi.org/10.1002/mgg3.501.