APA

Alatzoglou K. S., Turton J. P., Kelberman D., Clayton P. E., Mehta A., Buchanan C., Aylwin S., Crowne E. C., Christesen H. T., Hertel N. T., Trainer P. J., Savage M. O., Raza J., Banerjee K., Sinha S. K., Ten S., Mushtaq T., Brauner R., Cheetham T. D., Hindmarsh P. C., Mullis P. E. & Dattani M. T. (20090923). Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency. : The Journal of clinical endocrinology and metabolism.

Chicago

Alatzoglou Kyriaki S, Turton James P, Kelberman Daniel, Clayton Peter E, Mehta Ameeta, Buchanan Charles, Aylwin Simon, Crowne Elisabeth C, Christesen Henrik T, Hertel Niels T, Trainer Peter J, Savage Martin O, Raza Jamal, Banerjee Kausik, Sinha Sunil K, Ten Svetlana, Mushtaq Talat, Brauner Raja, Cheetham Timothy D, Hindmarsh Peter C, Mullis Primus E and Dattani Mehul T. 20090923. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency. : The Journal of clinical endocrinology and metabolism.

Harvard

Alatzoglou K. S., Turton J. P., Kelberman D., Clayton P. E., Mehta A., Buchanan C., Aylwin S., Crowne E. C., Christesen H. T., Hertel N. T., Trainer P. J., Savage M. O., Raza J., Banerjee K., Sinha S. K., Ten S., Mushtaq T., Brauner R., Cheetham T. D., Hindmarsh P. C., Mullis P. E. and Dattani M. T. (20090923). Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency. : The Journal of clinical endocrinology and metabolism.

MLA

Alatzoglou Kyriaki S, Turton James P, Kelberman Daniel, Clayton Peter E, Mehta Ameeta, Buchanan Charles, Aylwin Simon, Crowne Elisabeth C, Christesen Henrik T, Hertel Niels T, Trainer Peter J, Savage Martin O, Raza Jamal, Banerjee Kausik, Sinha Sunil K, Ten Svetlana, Mushtaq Talat, Brauner Raja, Cheetham Timothy D, Hindmarsh Peter C, Mullis Primus E and Dattani Mehul T. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency. : The Journal of clinical endocrinology and metabolism. 20090923.