Study of WT1, NPHS1 and NPHS2 in children with nephrotic syndrome
Comprehensive genetic and epigenetic investigation of patients with syndromic cent...
Detection of fetal genetic disorders through non-invasive prenatal testing using n...
Comprehensive genetic investigation of patients with Central Precocious Puberty as...
Investigation of osteogenesis, chondrogenesis, and phenotype rescue in Treacher Co...