A, V., A, O., V, B., B, T., A, B., F, S., . . . G, S. (2012). Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsy. European journal of medical genetics, 55(5), 362. https://doi.org/10.1016/j.ejmg.2012.03.011
Chicago Style (17th ed.) CitationA, Valetto, et al. "Molecular Cytogenetic Characterization of an Interstitial Deletion of Chromosome 21 (21q22.13q22.3) in a Patient with Dysmorphic Features, Intellectual Disability and Severe Generalized Epilepsy." European Journal of Medical Genetics 55, no. 5 (2012): 362. https://doi.org/10.1016/j.ejmg.2012.03.011.
MLA (9th ed.) CitationA, Valetto, et al. "Molecular Cytogenetic Characterization of an Interstitial Deletion of Chromosome 21 (21q22.13q22.3) in a Patient with Dysmorphic Features, Intellectual Disability and Severe Generalized Epilepsy." European Journal of Medical Genetics, vol. 55, no. 5, 2012, p. 362, https://doi.org/10.1016/j.ejmg.2012.03.011.