Search

Search Constraints

You searched for: Journal BMC endocrine disorders

Search Results

2. A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome. Issue 1 (December 2015)

3. A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans. Issue 1 (December 2016)

6. A randomised, open-labelstudy of insulin glargine or neutral protamine Hagedorn insulin in Chinese paediatric patients with type 1 diabetes mellitus. Issue 1 (December 2016)