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Archivos Argentinos De Pediatria|May 8, 2019
[Fragile X syndrome and other entities associated with the FMR1 gene: Study of 28 affected families]Mariel Ormazábal, Andrea Solari, Lucía Espeche, et al.Archivos Argentinos De Pediatria|November 1, 2017
[16p11.2 Microdeletion: first report in Argentina]Agostina Tardivo, Bárbara Masotto, Lucía Espeche, et al.Cytogenetic and Genome Research|December 2, 2019
Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital AnomaliesLucía S Massara, Marisol Delea, Lucía Espeche, et al.Pageof 1