Search for mutations in C-type natriuretic peptide receptor gene (NPR2) in individ...
Molecular diagnosis of the alterations in the GHRH-GH-IGF-1 axis in patients with ...
Phenotype related with p.L142fsX161 STAT5B mutation in the heterozygous state
Gene therapy by electrotransfer of mouse growth hormone gene in an animal model of...
Molecular analysis of LHX3 gene in patients with isolated or combined deficiency o...
Evaluate the response of the growth hormone treatment in children with idiopathic ...
Analysis of the lipids and carbohydrates metabolisms in Noonan syndrome patients