APA (7th ed.) Citation

Sakazume, S., Ohashi, H., Sasaki, Y., Harada, N., Nakanishi, K., Sato, H., . . . Kubota, T. (2012). Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation. Human genetics, 131(1), 121-130. https://doi.org/10.1007/s00439-011-1051-4

Chicago Style (17th ed.) Citation

Sakazume, Satoru, et al. "Spread of X-chromosome Inactivation into Chromosome 15 Is Associated with Prader–Willi Syndrome Phenotype in a Boy with a T(X;15)(p21.1;q11.2) Translocation." Human Genetics 131, no. 1 (2012): 121-130. https://doi.org/10.1007/s00439-011-1051-4.

MLA (9th ed.) Citation

Sakazume, Satoru, et al. "Spread of X-chromosome Inactivation into Chromosome 15 Is Associated with Prader–Willi Syndrome Phenotype in a Boy with a T(X;15)(p21.1;q11.2) Translocation." Human Genetics, vol. 131, no. 1, 2012, pp. 121-130, https://doi.org/10.1007/s00439-011-1051-4.