APA引文

Haack, T., Hogarth, P., Kruer, M., Gregory, A., Wieland, T., Schwarzmayr, T., . . . Hayflick, S. (2012). Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA. Elsevier.

Citação norma Chicago

Haack, Tobias B., et al. Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA. Elsevier, 2012.

MLA引文

Haack, Tobias B., et al. Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA. Elsevier, 2012.