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The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center studyJ D Cogan, B Ramel, M Lehto, et al.
Diabetes & Metabolism|July 4, 2017
Family history of type 1 and type 2 diabetes and risk of latent autoimmune diabetes in adults (LADA)R Hjort, L Alfredsson, T Andersson, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|July 4, 2012
Telomere length in blood and skeletal muscle in relation to measures of glycaemia and insulinaemiaS Ahmad, A Heraclides, Q Sun, et al.
Diabetes|January 19, 1999
Clinical and genetic characteristics of type 2 diabetes with and without GAD antibodiesT Tuomi, A Carlsson, H Li, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 21, 2007
Large-scale association study between two coding LRP5 gene polymorphisms and bone phenotypes and fractures in menE Grundberg, E M Lau, M Lorentzon, et al.
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