APA (7th ed.) Citation

Schlögel, M. J., Mendola, A., Fastré, E., Vasudevan, P., Devriendt, K., de Ravel, T. J., . . . Brouillard, P. (2015). No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome. Orphanet Journal of Rare Diseases, 10(1), 52. https://doi.org/10.1186/s13023-015-0271-4

Chicago Style (17th ed.) Citation

Schlögel, Matthieu J., et al. "No Evidence of Locus Heterogeneity in Familial Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation Syndrome." Orphanet Journal of Rare Diseases 10, no. 1 (2015): 52. https://doi.org/10.1186/s13023-015-0271-4.

MLA (9th ed.) Citation

Schlögel, Matthieu J., et al. "No Evidence of Locus Heterogeneity in Familial Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation Syndrome." Orphanet Journal of Rare Diseases, vol. 10, no. 1, 2015, p. 52, https://doi.org/10.1186/s13023-015-0271-4.