Vanesa Lotersztein

Acitretin embryopathy: A case report

Pablo Barbero, Vanesa Lotersztein, Rubén Bronberg et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2004 · 41 citations

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

Jair Tenorio, Pablo Alarcón, Pedro Arias et al. · European Journal of Human Genetics · 2019 · 30 citations · Full text

New Patients, Mendelian Disorder, Genetic Disorder +9

<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

GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort

Paula I. Buonfiglio, Carlos David Bruque, Leonela Luce et al. · Genes · 2020 · 18 citations · Full text