Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 9, 2005
An autosomal dominant high bone mass phenotype in association with craniosynostosis in an extended family is caused by an LRP5 missense mutationMei Lan Kwee, Wendy Balemans, Erna Cleiren, et al.
Diabetes Care|May 7, 2008
Short-term hyperglycemic dysregulation in patients with type 1 diabetes does not change myocardial triglyceride content or myocardial functionSebastiaan Hammer, Jacqueline T Jonker, Hildo J Lamb, et al.
The Journal of Clinical Endocrinology and Metabolism|January 15, 2002
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918Fred H Menko, Rob B van der Luijt, Irene A J de Valk, et al.
Pageof 1