Cita APA

O'Sullivan, J., Bitu, C., Daly, S., Urquhart, J., Barron, M., Bhaskar, S., . . . Dixon, M. (2011). Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome. Elsevier.

Citación estilo Chicago

O'Sullivan, James, et al. Whole-Exome Sequencing Identifies FAM20A Mutations As a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome. Elsevier, 2011.

Cita MLA

O'Sullivan, James, et al. Whole-Exome Sequencing Identifies FAM20A Mutations As a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome. Elsevier, 2011.