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
Genotype-Phenotype Correlations in Patients with Hereditary Angioedema
Standardization of total RNA extraction and amplification for the analysis of long...
Standardization of PCR and sequencing methods for DNA methylation analysis of LDLR...