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Page 1
Tall stature in familial glucocorticoid deficiency.
Elias LL, Huebner A, Metherell LA, Canas A, Warne GL, Bitti ML, Cianfarani S, Clayton PE, Savage MO, Clark AJ. Elias LL, et al. Among authors: clayton pe. Clin Endocrinol (Oxf). 2000 Oct;53(4):423-30. doi: 10.1046/j.1365-2265.2000.01122.x. Clin Endocrinol (Oxf). 2000. PMID: 11012566
Biochemical tests in the diagnosis of childhood growth hormone deficiency.
Tillmann V, Buckler JM, Kibirige MS, Price DA, Shalet SM, Wales JK, Addison MG, Gill MS, Whatmore AJ, Clayton PE. Tillmann V, et al. Among authors: clayton pe. J Clin Endocrinol Metab. 1997 Feb;82(2):531-5. doi: 10.1210/jcem.82.2.3750. J Clin Endocrinol Metab. 1997. PMID: 9024249
Serum leptin through childhood and adolescence.
Clayton PE, Gill MS, Hall CM, Tillmann V, Whatmore AJ, Price DA. Clayton PE, et al. Clin Endocrinol (Oxf). 1997 Jun;46(6):727-33. doi: 10.1046/j.1365-2265.1997.2081026.x. Clin Endocrinol (Oxf). 1997. PMID: 9274704
New growth hormone receptor exon 9 mutation causes genetic short stature.
Ayling RM, Ross RJ, Towner P, Von Laue S, Finidori J, Moutoussamy S, Buchanan CR, Clayton PE, Norman MR. Ayling RM, et al. Among authors: clayton pe. Acta Paediatr Suppl. 1999 Feb;88(428):168-72; discussion 173. doi: 10.1111/j.1651-2227.1999.tb14380.x. Acta Paediatr Suppl. 1999. PMID: 10102075
282 results