APA (7th ed.) Citation

Ogata, T., Niihori, T., Tanaka, N., Kawai, M., Nagashima, T., Funayama, R., . . . Matsubara, Y. (2014). TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia. PloS one, 9(3), e91598. https://doi.org/10.1371/journal.pone.0091598

Chicago Style (17th ed.) Citation

Ogata, Tsutomu, et al. "TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia." PloS One 9, no. 3 (2014): e91598. https://doi.org/10.1371/journal.pone.0091598.

MLA (9th ed.) Citation

Ogata, Tsutomu, et al. "TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia." PloS One, vol. 9, no. 3, 2014, p. e91598, https://doi.org/10.1371/journal.pone.0091598.