Molecular diagnosis of the alterations in the GHRH-GH-IGF-1 axis in patients with ...
Xia-Gibbs syndrome: molecular and clinical characterization of a series of Brazil...
Genetic and pathophysiological mechanisms in mendelian neurodevelopmental disorder...
Identification of predisposition genes associated with breast and thyroid carcinom...
Genetic analysis of patients with arrhythmogenic right ventricular dysplasia (ARVD...
FUNCTIONAL STUDY OF THE EHMT2 GENE (CANDIDATE FOR A NOVEL KLEEFSTRA-LIKE SYNDROME)