Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.

MLA

Westbury, Sarah K., et al. “Human Phenotype Ontology Annotation and Cluster Analysis to Unravel Genetic Defects in 707 Cases with Unexplained Bleeding and Platelet Disorders.” Genome Medicine, vol. 7, no. 1, May 2015, pp. 1–15. EBSCOhost, https://doi.org/10.1186/s13073-015-0151-5.

APA

Westbury, S. K., Turro, E., Greene, D., Lentaigne, C., Kelly, A. M., Bariana, T. K., Simeoni, I., Pillois, X., Attwood, A., Austin, S., Jansen, S. B. G., Bakchoul, T., Crisp-Hihn, A., Erber, W. N., Favier, R., Foad, N., Gattens, M., Jolley, J. D., Liesner, R., & Meacham, S. (2015). Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders. Genome Medicine, 7(1), 1–15. https://doi.org/10.1186/s13073-015-0151-5

Chicago

Westbury, Sarah K., Ernest Turro, Daniel Greene, Claire Lentaigne, Anne M. Kelly, Tadbir K. Bariana, Ilenia Simeoni, et al. 2015. “Human Phenotype Ontology Annotation and Cluster Analysis to Unravel Genetic Defects in 707 Cases with Unexplained Bleeding and Platelet Disorders.” Genome Medicine 7 (1): 1–15. doi:10.1186/s13073-015-0151-5.