Buscar por Autor Laiseca, Julieta
Mostrando resultados 1 a 2 de 2
| Fecha de publicación | Título | Autor(es) |
|---|---|---|
| 4-sep-2025 | Classic Prader-Willi Syndrome Phenotype Caused by an Atypical Deletion in the 15q11 Region Not Involving the SNORD Genes | Martínez, Jazmín Belén ; Arancedo, Josefina María Álvarez ; Solari, Andrea ; Claps, Aldana ; Castro, Tania ; Laiseca, Julieta ; Taboas, Melisa |
| 10-jul-2025 | High precision characterization of RCCX rearrangements in a 21-hydroxylase deficiency Latin American cohort using oxford nanopore long read sequencing | Claps, Aldana ; Kolomenski, Emilio ; Fernández, Franco ; Macchiaroli, Natalia ; Ingravidi, Marina ; Delea, Marisol ; Fernandez, Cecilia ; Castro, Tania ; Laiseca, Julieta ; Kamenetzky, Laura ; Taboas, Melisa ; Dain, Liliana |

