Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.

MLA

Xavier Estivill, and Lluís Armengol. “Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies.” PLoS Genetics, vol. 3, no. 10, Oct. 2007, pp. 1787–99. EBSCOhost, https://doi.org/10.1371/journal.pgen.0030190.

APA

Xavier Estivill, & Lluís Armengol. (2007). Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies. PLoS Genetics, 3(10), 1787–1799. https://doi.org/10.1371/journal.pgen.0030190

Chicago

Xavier Estivill, and Lluís Armengol. 2007. “Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies.” PLoS Genetics 3 (10): 1787–99. doi:10.1371/journal.pgen.0030190.