APA (7th ed.) Citation

PF, G., L, A., A, S., RD, B., J, L., CL, R., . . . U, B. (2015). Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes. American journal of medical genetics. Part A, 167A(1), 95. https://doi.org/10.1002/ajmg.a.36799

Chicago Style (17th ed.) Citation

PF, Giampietro, et al. "Whole Exome Sequencing Identifies a POLRID Mutation Segregating in a Father and Two Daughters with Findings of Klippel-Feil and Treacher Collins Syndromes." American Journal of Medical Genetics. Part A 167A, no. 1 (2015): 95. https://doi.org/10.1002/ajmg.a.36799.

MLA (9th ed.) Citation

PF, Giampietro, et al. "Whole Exome Sequencing Identifies a POLRID Mutation Segregating in a Father and Two Daughters with Findings of Klippel-Feil and Treacher Collins Syndromes." American Journal of Medical Genetics. Part A, vol. 167A, no. 1, 2015, p. 95, https://doi.org/10.1002/ajmg.a.36799.