APA (7th ed.) Citation

Schönewolf‐Greulich, B., Tejada, M., Stephens, K., Hadzsiev, K., Gauthier, J., Brøndum‐Nielsen, K., . . . Tümer, Z. (2016). The MECP2 variant c. 925C>T (p. Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome. Clinical Genetics, 89(6), 733. https://doi.org/10.1111/cge.12769

Chicago Style (17th ed.) Citation

Schönewolf‐Greulich, B., et al. "The MECP2 Variant C. 925C>T (p. Arg309Trp) Causes Intellectual Disability in Both Males and Females Without Classic Features of Rett Syndrome." Clinical Genetics 89, no. 6 (2016): 733. https://doi.org/10.1111/cge.12769.

MLA (9th ed.) Citation

Schönewolf‐Greulich, B., et al. "The MECP2 Variant C. 925C>T (p. Arg309Trp) Causes Intellectual Disability in Both Males and Females Without Classic Features of Rett Syndrome." Clinical Genetics, vol. 89, no. 6, 2016, p. 733, https://doi.org/10.1111/cge.12769.