Cecilia Fernández

Structure-Based Analysis of Five Novel Disease-Causing Mutations in 21-Hydroxylase-Deficient Patients

Carolina Minutolo, Alejandro D. Nadra, Cecilia Fernández et al. · PLoS ONE · 2011 · 30 citations · Full text

Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations

Carlos David Bruque, Marisol Delea, Cecilia Fernández et al. · Scientific Reports · 2016 · 21 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

Loss of Heterozygosity on the Short Arm of Chromosome 3 in Renal Cancer

M.L. Maestro, V. del Barco, María Teresa Sanz Casla et al. · Oncology · 2000 · 16 citations

Cancer Pathology, Cytogenetics, Genetics +20

First custom next-generation sequencing infertility panel in Latin America: design and first results

Daniela Lorenzi, Cecilia Fernández, Melina Bilinski et al. · JBRA · 2020 · 16 citations · Full text