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Results 1-3 of 3 (Search time: 0.001 seconds).

Issue DateTitleAuthor(s)
14-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 
210-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 
31-Oct-2023Novel variant in the KAT6B gene associated with Say Barber Biesecker Young SimpsonSolari, Andrea ; Alberto, Guillermo ; Benitez Medina, Ana ; García Ayré, Brenda ; Parisini, Daniel ; Claps, Aldana ; Taboas, Melisa