Cite
Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation.
MLA
Tomaselli, Sara, et al. “Syndromic True Hermaphroditism Due to an R-Spondin1 (RSPO1) Homozygous Mutation.” Human Mutation, vol. 29, no. 2, Feb. 2008, pp. 220–26. EBSCOhost, https://doi.org/10.1002/humu.20665.
APA
Tomaselli, S., Megiorni, F., De Bernardo, C., Felici, A., Marrocco, G., Maggiulli, G., Grammatico, B., Remotti, D., Saccucci, P., Valentini, F., Mazzilli, M. C., Majore, S., & Grammatico, P. (2008). Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation. Human Mutation, 29(2), 220–226. https://doi.org/10.1002/humu.20665
Chicago
Tomaselli, Sara, Francesca Megiorni, Carmelilia De Bernardo, Aldo Felici, Giacinto Marrocco, Giorgio Maggiulli, Barbara Grammatico, et al. 2008. “Syndromic True Hermaphroditism Due to an R-Spondin1 (RSPO1) Homozygous Mutation.” Human Mutation 29 (2): 220–26. doi:10.1002/humu.20665.