APA (7th ed.) Citation

P, A., J, G., AB, B., TSE, H., M, B., J, F., . . . HS, S. (2020). Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome. American journal of medical genetics. Part A, 182(5), 1273. https://doi.org/10.1002/ajmg.a.61541

Chicago Style (17th ed.) Citation

P, Arts, et al. "Paternal Mosaicism for a Novel PBX1 Mutation Associated with Recurrent Perinatal Death: Phenotypic Expansion of the PBX1-related Syndrome." American Journal of Medical Genetics. Part A 182, no. 5 (2020): 1273. https://doi.org/10.1002/ajmg.a.61541.

MLA (9th ed.) Citation

P, Arts, et al. "Paternal Mosaicism for a Novel PBX1 Mutation Associated with Recurrent Perinatal Death: Phenotypic Expansion of the PBX1-related Syndrome." American Journal of Medical Genetics. Part A, vol. 182, no. 5, 2020, p. 1273, https://doi.org/10.1002/ajmg.a.61541.