APA (7th ed.) Citation

G, G., R, M., JE, S., & D, B. (2022). A severe case of Bosch-Boonstra-Schaaf optic atrophy syndrome with a novel description of coloboma and septo-optic dysplasia, owing to a start codon variant in the NR2F1 gene. American journal of medical genetics. Part A, 188(3), 900. https://doi.org/10.1002/ajmg.a.62569

Chicago Style (17th ed.) Citation

G, Gazdagh, Mawby R, Self JE, and Baralle D. "A Severe Case of Bosch-Boonstra-Schaaf Optic Atrophy Syndrome with a Novel Description of Coloboma and Septo-optic Dysplasia, Owing to a Start Codon Variant in the NR2F1 Gene." American Journal of Medical Genetics. Part A 188, no. 3 (2022): 900. https://doi.org/10.1002/ajmg.a.62569.

MLA (9th ed.) Citation

G, Gazdagh, et al. "A Severe Case of Bosch-Boonstra-Schaaf Optic Atrophy Syndrome with a Novel Description of Coloboma and Septo-optic Dysplasia, Owing to a Start Codon Variant in the NR2F1 Gene." American Journal of Medical Genetics. Part A, vol. 188, no. 3, 2022, p. 900, https://doi.org/10.1002/ajmg.a.62569.