APA (7th ed.) Citation

Haverkämper, S., Marquardt, T., Haußer-Siller, I., Timme, K., Kuehn, T., Hertzberg, C., & Rossi, R. (2011). Congenital ichthyosis in severe type II Gaucher disease with a homozygous null mutation. Neonatology, 100(2), . https://doi.org/10.1159/000324116

Chicago Style (17th ed.) Citation

Haverkämper, Sabine, Thorsten Marquardt, Ingrid Haußer-Siller, Katharina Timme, Thomas Kuehn, Christoph Hertzberg, and Rainer Rossi. "Congenital Ichthyosis in Severe Type II Gaucher Disease with a Homozygous Null Mutation." Neonatology 100, no. 2 (2011). https://doi.org/10.1159/000324116.

MLA (9th ed.) Citation

Haverkämper, Sabine, et al. "Congenital Ichthyosis in Severe Type II Gaucher Disease with a Homozygous Null Mutation." Neonatology, vol. 100, no. 2, 2011, https://doi.org/10.1159/000324116.