APA

McInerney-Leo A. M., Marshall M. S., Gardiner B., Benn D. E., McFarlane J., Robinson B. G., Brown M. A., Leo P. J., Clifton-Bligh R. J. & Duncan E. L. (20140729). Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. : Clinical endocrinology.

Chicago

McInerney-Leo Aideen M, Marshall Mhairi S, Gardiner Brooke, Benn Diana E, McFarlane Janelle, Robinson Bruce G, Brown Matthew A, Leo Paul J, Clifton-Bligh Roderick J and Duncan Emma L. 20140729. Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. : Clinical endocrinology.

Harvard

McInerney-Leo A. M., Marshall M. S., Gardiner B., Benn D. E., McFarlane J., Robinson B. G., Brown M. A., Leo P. J., Clifton-Bligh R. J. and Duncan E. L. (20140729). Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. : Clinical endocrinology.

MLA

McInerney-Leo Aideen M, Marshall Mhairi S, Gardiner Brooke, Benn Diana E, McFarlane Janelle, Robinson Bruce G, Brown Matthew A, Leo Paul J, Clifton-Bligh Roderick J and Duncan Emma L. Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. : Clinical endocrinology. 20140729.