APA

Faridi R., Rehman A. U., Morell R. J., Friedman P. L., Demain L., Zahra S., Khan A. A., Tohlob D., Assir M. Z., Beaman G., Khan S. N., Newman W. G., Riazuddin S. & Friedman T. B. (20170626). Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. : Clinical genetics.

Chicago

Faridi R, Rehman A U, Morell R J, Friedman P L, Demain L, Zahra S, Khan A A, Tohlob D, Assir M Z, Beaman G, Khan S N, Newman W G, Riazuddin S and Friedman T B. 20170626. Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. : Clinical genetics.

Harvard

Faridi R., Rehman A. U., Morell R. J., Friedman P. L., Demain L., Zahra S., Khan A. A., Tohlob D., Assir M. Z., Beaman G., Khan S. N., Newman W. G., Riazuddin S. and Friedman T. B. (20170626). Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. : Clinical genetics.

MLA

Faridi R, Rehman A U, Morell R J, Friedman P L, Demain L, Zahra S, Khan A A, Tohlob D, Assir M Z, Beaman G, Khan S N, Newman W G, Riazuddin S and Friedman T B. Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. : Clinical genetics. 20170626.