APA (7th ed.) Citation

N, G., SW, G., DR, D., & PJ, T. (2021). Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant. Journal of clinical research in pediatric endocrinology, 13(2), 218. https://doi.org/10.4274/jcrpe.galenos.2020.2020.0012

Chicago Style (17th ed.) Citation

N, Gupta, Gregory SW, Deyle DR, and Tebben PJ. "Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta Due to a COL1A1 Variant." Journal of Clinical Research in Pediatric Endocrinology 13, no. 2 (2021): 218. https://doi.org/10.4274/jcrpe.galenos.2020.2020.0012.

MLA (9th ed.) Citation

N, Gupta, et al. "Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta Due to a COL1A1 Variant." Journal of Clinical Research in Pediatric Endocrinology, vol. 13, no. 2, 2021, p. 218, https://doi.org/10.4274/jcrpe.galenos.2020.2020.0012.