Massive-parallel sequencing by gene panel in the diagnosis of congenital hypopit...

Growth hormone secretatogue receptor gene (GHSR) analysis in patients with idiopathic...

Growth pattern of patients with Noonan syndrome with identified mutations in PTPN11,...

Integrated molecular genetic analysis applied to the investigation process of patients...

Study of STAT5B mutation in Criciúma - Santa Catarina: frequency and phenotypic characterization...

Heterozygous mutations in natriuretic peptide receptor-B gene (NPR2) are cause of...