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Nombre completo
Delea, Marisol
Publicaciones
(Artículos)
Resultados 1-8 de 8.
| Fecha de publicación | Título | Autor(es) | |
|---|---|---|---|
| 1 | 26-mar-2019 | A novel pathogenic frameshift variant of KAT6B identified by clinical exome sequencing in a newborn with the Say-Barber-Biesecker-Young-Simpson syndrome | Mendez, Rodrigo ; Delea, Marisol ; Dain, Liliana ; Rittler, Mónica |
| 2 | jul-2020 | An update on genetic variants of the NKX2-5 | Delea, Marisol ; Simonetti, Leandro ; Fabbro, Mónica ; Espeche, Lucía ; Taboas, Melisa ; Nadra, Alejandro D. ; Bruque, Carlos David ; Dain, Liliana |
| 3 | 11-feb-2021 | Análisis de anomalías cromosómicas, desbalances genómicos y variantes de secuencia como causa de cardiopatías congénitas | Delea, Marisol ; Massara, Soledad ; Bruque, Carlos David ; Espeche, Lucía ; Taboas, Melisa ; Barbero, Pablo ; Bidondo, María Paz ; Liascovich, Rosa ; Groisman, Boris ; Cosentino, Viviana R ; Martinoli, Celeste ; Furforo, Lilian ; Ritler, Mónica ; Kolomenski, Emilio ; Oliveri, Jaen ; Brun, Paloma ; Rozental, Sandra ; Dain, Liliana |
| 4 | 16-ago-2017 | Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency | Espeche, Lucía ; Chiauzzi, Violeta ; Ferder, Ianina ; Arrar, Mehrnoosh ; Solari, Andrea ; Bruque, Carlos David ; Delea, Marisol ; Belli, Susana ; Fernández, Cecilia Soledad ; Buzzalino, Noemí Delia ; Charreau, Eduardo Hernán ; Dain, Liliana |
| 5 | 22-jun-2022 | Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease | Delea, Marisol ; Massara, Lucía S ; Espeche, Lucía ; Bidondo, Maria Paz ; Barbero, Pablo ; Oliveri, Jaen ; Brun, Paloma ; Fabro, Mónica ; Galain, Micaela ; Fernandez, Cecilia ; Taboas, Melisa ; Bruque, Carlos David ; Kolomenski, Emilio ; Izquiedo, Agustín ; Berenstein, Ariel ; Cosentino, Viviana R ; Martinoli, Celeste ; Vilas, Mariana ; Rittler, Mónica ; Mendez, Rodrigo ; Furforo, Lilian ; Liascovich, Rosa ; Groisman, Boris ; Rozental, Sandra ; Dain, Liliana |
| 6 | 11-sep-2018 | Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects | Delea, Marisol ; Espeche, Lucía ; Bruque, Carlos David ; Bidondo, María Paz ; Massara, Lucía S ; Oliveri, Jaen ; Brun, Paloma ; Cosentino, Viviana R ; Martinoli, Celeste ; Tolaba, Norma ; Picon, Claudina ; Ponce Zaldua, María Eugenia ; Ávila, Silvia ; Gutnisky, Viviana ; Pérez, Myriam ; Furforo, Lilian ; Buzzalino, Noemí Delia ; Liascovich, Rosa ; Groisman, Boris ; Rittler, Mónica ; Rozental, Sandra ; Barbero, Pablo ; Dain, Liliana |
| 7 | 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 |
| 8 | dic-2016 | Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations | Bruque, Carlos David ; Delea, Marisol ; Fernández, Cecilia ; Orza, Juan V ; Taboas, Melisa ; Buzzalino, Noemí ; Espeche, Lucía ; Solari, Andrea ; Luccerini, Verónica ; Alba, Liliana ; Nadra, Alejandro D. ; Dain, Liliana |