Dimassi, S., Labalme, A., Ville, D., Calender, A., Mignot, C., Boutry‐Kryza, N., . . . Sanlaville, D. (2016). Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome. Clinical Genetics, 89(2), 198. https://doi.org/10.1111/cge.12636
Chicago Style (17th ed.) CitationDimassi, S., et al. "Whole-exome Sequencing Improves the Diagnosis Yield in Sporadic Infantile Spasm Syndrome." Clinical Genetics 89, no. 2 (2016): 198. https://doi.org/10.1111/cge.12636.
MLA (9th ed.) CitationDimassi, S., et al. "Whole-exome Sequencing Improves the Diagnosis Yield in Sporadic Infantile Spasm Syndrome." Clinical Genetics, vol. 89, no. 2, 2016, p. 198, https://doi.org/10.1111/cge.12636.
Warning: These citations may not always be 100% accurate.