APA

Hess O., Hujeirat Y., Wajnrajch M. P., Allon-Shalev S., Zadik Z., Lavi I. & Tenenbaum-Rakover Y. (20080102). Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene. : The Journal of clinical endocrinology and metabolism.

Chicago

Hess Ora, Hujeirat Yasir, Wajnrajch Michael P, Allon-Shalev Stavit, Zadik Zvi, Lavi Idit and Tenenbaum-Rakover Yardena. 20080102. Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene. : The Journal of clinical endocrinology and metabolism.

Harvard

Hess O., Hujeirat Y., Wajnrajch M. P., Allon-Shalev S., Zadik Z., Lavi I. and Tenenbaum-Rakover Y. (20080102). Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene. : The Journal of clinical endocrinology and metabolism.

MLA

Hess Ora, Hujeirat Yasir, Wajnrajch Michael P, Allon-Shalev Stavit, Zadik Zvi, Lavi Idit and Tenenbaum-Rakover Yardena. Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene. : The Journal of clinical endocrinology and metabolism. 20080102.