APA (7th ed.) Citation

O, V., N, I., E, F., A, V., EA, V., D, G., . . . MI, T. (2018). Functional Analyses of a Novel Splice Variant in the CHD7 Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome. Frontiers in genetics, 9, 7. https://doi.org/10.3389/fgene.2018.00007

Chicago Style (17th ed.) Citation

O, Villate, Ibarluzea N, Fraile-Bethencourt E, Valenzuela A, Velasco EA, Grozeva D, Raymond FL, Botella MP, and Tejada MI. "Functional Analyses of a Novel Splice Variant in the CHD7 Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome." Frontiers in Genetics 9 (2018): 7. https://doi.org/10.3389/fgene.2018.00007.

MLA (9th ed.) Citation

O, Villate, et al. "Functional Analyses of a Novel Splice Variant in the CHD7 Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome." Frontiers in Genetics, vol. 9, 2018, p. 7, https://doi.org/10.3389/fgene.2018.00007.