एपीए उद्धरण

Brown, K., Selfridge, J., Lagger, S., Connelly, J., De Sousa, D., Kerr, A., . . . Bird, A. (2016). The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome. Hum Mol Genet.

शिकागो स्टाइल उद्धरण

Brown, Kyla, et al. "The Molecular Basis of Variable Phenotypic Severity Among Common Missense Mutations Causing Rett Syndrome." Hum Mol Genet 2016.

एमएलए उद्धरण

Brown, Kyla, et al. "The Molecular Basis of Variable Phenotypic Severity Among Common Missense Mutations Causing Rett Syndrome." Hum Mol Genet 2016.