Artículo especial
Desarrollo y aplicación de modelos predictivos en el síndrome de Lynch
Predictive models for identification of germline mutation carriers in Lynch syndrome
Isela Quispe, Judith Balmaña
Autor para correspondencia
Servicio de Oncología Médica, Hospital Universitario Vall d’Hebron, Departamento de Medicina Universitat Autònoma de Barcelona, Barcelona, España
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| 2023 3 | 3 | 0 | 3 |
| 2019 10 | 1 | 0 | 1 |
| 2017 10 | 16 | 4 | 20 |
| 2017 9 | 28 | 19 | 47 |
| 2017 8 | 31 | 5 | 36 |
| 2017 7 | 19 | 3 | 22 |
| 2017 6 | 26 | 15 | 41 |
| 2017 5 | 33 | 14 | 47 |
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| 2017 2 | 36 | 19 | 55 |
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| 2016 2 | 46 | 18 | 64 |
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| 2013 8 | 29 | 3 | 32 |
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| 2013 6 | 1 | 0 | 1 |
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| 2010 4 | 497 | 0 | 497 |
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