Browsing by Author Laiseca, Julieta

Showing results 1 to 2 of 2
Issue DateTitleAuthor(s)
4-Sep-2025Classic Prader-Willi Syndrome Phenotype Caused by an Atypical Deletion in the 15q11 Region Not Involving the SNORD GenesMartínez, Jazmín Belén ; Arancedo, Josefina María Álvarez ; Solari, Andrea ; Claps, Aldana ; Castro, Tania ; Laiseca, Julieta ; Taboas, Melisa 
10-Jul-2025High precision characterization of RCCX rearrangements in a 21-hydroxylase deficiency Latin American cohort using oxford nanopore long read sequencingClaps, Aldana ; Kolomenski, Emilio ; Fernández, Franco ; Macchiaroli, Natalia ; Ingravidi, Marina ; Delea, Marisol ; Fernandez, Cecilia ; Castro, Tania ; Laiseca, Julieta ; Kamenetzky, Laura ; Taboas, Melisa ; Dain, Liliana