APA citiranje

McInerney-Leo, A. M., Marshall, M. S., Gardiner, B., Coucke, P. J., Van Laer, L., Loeys, B. L., . . . Duncan, E. L. (2013). Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome. Nature Publishing Group.

Citação norma Chicago

McInerney-Leo, Aideen M., et al. Whole Exome Sequencing Is an Efficient, Sensitive and Specific Method of Mutation Detection in Osteogenesis Imperfecta and Marfan Syndrome. Nature Publishing Group, 2013.

MLA citiranje

McInerney-Leo, Aideen M., et al. Whole Exome Sequencing Is an Efficient, Sensitive and Specific Method of Mutation Detection in Osteogenesis Imperfecta and Marfan Syndrome. Nature Publishing Group, 2013.