Viviana Dalamón

Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients

Viviana Dalamón, Agustina Bèherán, Fernando Diamante et al. · Hearing Research · 2005 · 45 citations

Mendelian Disorder, Genetic Disorder, Genetics +9

Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy

Florencia Giliberto, Verónica Ferreiro, Viviana Dalamón et al. · Neurological Research · 2004 · 42 citations

<i>GJB2</i> and <i>GJB6</i> Genes: Molecular Study and Identification of Novel <i>GJB2</i> Mutations in the Hearing-Impaired Argentinean Population

Viviana Dalamón, Vanesa Lotersztein, Agustina Bèherán et al. · Audiology and Neurotology · 2009 · 23 citations · Full text

Predicting pathogenicity for novel hearing loss mutations based on genetic and protein structure approaches

Paula I. Buonfiglio, Carlos David Bruque, Vanesa Lotersztein et al. · Scientific Reports · 2022 · 23 citations · Full text

Detection of Germline Mutations in Argentine Retinoblastoma Patients: Low and Full Penetrance Retinoblastoma Caused by the Same Germline Truncating Mutation

Viviana Dalamón, Ezequiel Surace, Florencia Giliberto et al. · BMB Reports · 2004 · 19 citations · Full text

T Exonic Transitions, Somatic Variant, Bilateral Retinoblastoma Patients +9