APA

Borel C., Cheung F., Stewart H., Koolen D. A., Phillips C., Thomas N. S., Jacobs P. A., Eliez S. & Sharp A. J. (20121015). Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction. : Human genetics.

Chicago

Borel Christelle, Cheung Fanny, Stewart Helen, Koolen David A, Phillips Christopher, Thomas N Simon, Jacobs Patricia A, Eliez Stephan and Sharp Andrew J. 20121015. Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction. : Human genetics.

Harvard

Borel C., Cheung F., Stewart H., Koolen D. A., Phillips C., Thomas N. S., Jacobs P. A., Eliez S. and Sharp A. J. (20121015). Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction. : Human genetics.

MLA

Borel Christelle, Cheung Fanny, Stewart Helen, Koolen David A, Phillips Christopher, Thomas N Simon, Jacobs Patricia A, Eliez Stephan and Sharp Andrew J. Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction. : Human genetics. 20121015.