Characterization of gene duplication associated with nonsyndromic hearing loss
PREVALENCE OF STRC AND OTOA GENE PATHOGENIC DELETIONS AND VARIANTS IN BRAZILIAN PA...
Genetic and pathophysiological mechanisms in mendelian neurodevelopmental disorder...
Identification of novel genes and functional studies in nonsyndromic deafness
Hereditary angioedema: clinical and genetic study of a Brazilian family
Investigation of the molecular basis of familial non-medullary thyroid cancer.
Genotype-Phenotype Correlations in Patients with Hereditary Angioedema