APA (7th ed.) Citation

D'Amours, G., Kibar, Z., Mathonnet, G., Fetni, R., Tihy, F., Désilets, V., . . . Lemyre, E. (2012). Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype. Clinical Genetics, 81(2), 128. https://doi.org/10.1111/j.1399-0004.2011.01687.x

Chicago Style (17th ed.) Citation

D'Amours, G., Z. Kibar, G. Mathonnet, R. Fetni, F. Tihy, V. Désilets, S. Nizard, JL Michaud, and E. Lemyre. "Whole-genome Array CGH Identifies Pathogenic Copy Number Variations in Fetuses with Major Malformations and a Normal Karyotype." Clinical Genetics 81, no. 2 (2012): 128. https://doi.org/10.1111/j.1399-0004.2011.01687.x.

MLA (9th ed.) Citation

D'Amours, G., et al. "Whole-genome Array CGH Identifies Pathogenic Copy Number Variations in Fetuses with Major Malformations and a Normal Karyotype." Clinical Genetics, vol. 81, no. 2, 2012, p. 128, https://doi.org/10.1111/j.1399-0004.2011.01687.x.