Sanders, S. J. Et Al. 2012. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. NATURE , vol.485, no.7397 , 237-241.

Sanders, S. J., Murtha, M. T., Gupta, A. R., Murdoch, J. D., Raubeson, M. J., Willsey, A. J., ... Ercan-Sencicek, A. G.(2012). De novo mutations revealed by whole-exome sequencing are strongly associated with autism. NATURE , vol.485, no.7397, 237-241.

Sanders, Stephan Et Al. "De novo mutations revealed by whole-exome sequencing are strongly associated with autism," NATURE , vol.485, no.7397, 237-241, 2012

Sanders, Stephan J. Et Al. "De novo mutations revealed by whole-exome sequencing are strongly associated with autism." NATURE , vol.485, no.7397, pp.237-241, 2012

Sanders, S. J. Et Al. (2012) . "De novo mutations revealed by whole-exome sequencing are strongly associated with autism." NATURE , vol.485, no.7397, pp.237-241.

@article{article, author={Stephan J. Sanders Et Al. }, title={De novo mutations revealed by whole-exome sequencing are strongly associated with autism}, journal={NATURE}, year=2012, pages={237-241} }