APA

Carr I. M., Morgan J., Watson C., Melnik S., Diggle C. P., Logan C. V., Harrison S. M., Taylor G. R., Pena S. D. J., Markham A. F., Alkuraya F. S., Black G. C. M., Ali M. & Bonthron D. T. (20140127). Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data. : Human mutation.

Chicago

Carr Ian M, Morgan Joanne, Watson Christopher, Melnik Svitlana, Diggle Christine P, Logan Clare V, Harrison Sally M, Taylor Graham R, Pena Sergio D J, Markham Alexander F, Alkuraya Fowzan S, Black Graeme C M, Ali Manir and Bonthron David T. 20140127. Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data. : Human mutation.

Harvard

Carr I. M., Morgan J., Watson C., Melnik S., Diggle C. P., Logan C. V., Harrison S. M., Taylor G. R., Pena S. D. J., Markham A. F., Alkuraya F. S., Black G. C. M., Ali M. and Bonthron D. T. (20140127). Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data. : Human mutation.

MLA

Carr Ian M, Morgan Joanne, Watson Christopher, Melnik Svitlana, Diggle Christine P, Logan Clare V, Harrison Sally M, Taylor Graham R, Pena Sergio D J, Markham Alexander F, Alkuraya Fowzan S, Black Graeme C M, Ali Manir and Bonthron David T. Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data. : Human mutation. 20140127.