Study of the phenotype associated to heterozigous STAT5B mutation p.L142fsX161
Molecular analysis of LHX3 gene in patients with isolated or combined deficiency o...
Search for mutations in C-type natriuretic peptide receptor gene (NPR2) in individ...
Genetic analysis and mechanisms of modulation of congenital hypopituitarism phenot...
Gene therapy by electrotransfer of mouse growth hormone gene in an animal model of...
Role of GH use in the development of ACTH-producing macroadenoma in a patient with...
New approaches and methodologies in molecular-genetic studies of growth and pubert...