APA (7th ed.) Citation

van Rahden, V. A., Rau, I., Fuchs, S., Kosyna, F. K., de Almeida Jr, H. L., Fryssira, H., . . . Kutsche, K. (2014). Clinical spectrum of females with HCCS mutation: From no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome. Orphanet Journal of Rare Diseases, 9(1), 3. https://doi.org/10.1186/1750-1172-9-53

Chicago Style (17th ed.) Citation

van Rahden, Vanessa A., et al. "Clinical Spectrum of Females with HCCS Mutation: From No Clinical Signs to a Neonatal Lethal Form of the Microphthalmia with Linear Skin Defects (MLS) Syndrome." Orphanet Journal of Rare Diseases 9, no. 1 (2014): 3. https://doi.org/10.1186/1750-1172-9-53.

MLA (9th ed.) Citation

van Rahden, Vanessa A., et al. "Clinical Spectrum of Females with HCCS Mutation: From No Clinical Signs to a Neonatal Lethal Form of the Microphthalmia with Linear Skin Defects (MLS) Syndrome." Orphanet Journal of Rare Diseases, vol. 9, no. 1, 2014, p. 3, https://doi.org/10.1186/1750-1172-9-53.