Five Years of Multidisciplinary Care in Hereditary Cancer: Our Experience in a Spanish University Hospital

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dc.contributor.authorIván Márquez‐Rodas
dc.contributor.authorMiriam Lobo
dc.contributor.authorCésar Manuel Flores-Sánchez
dc.contributor.authorM.T. Sanz
dc.contributor.authorSònia Luque
dc.contributor.authorSantiago Lizarraga
dc.contributor.authorCecilia González-Asanza
dc.contributor.authorJ.A. Pajares
dc.contributor.authorMaría Isabel Peligros
dc.contributor.authorOscar Bueno
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T15:15:58Z
dc.date.available2026-03-22T15:15:58Z
dc.date.issued2016
dc.descriptionCitaciones: 3
dc.description.abstractWe have a high mutation detection rate, genetic test acceptance, and compliance with risk reduction strategies. However, there is room for improvement, especially in genetic testing timing, considering that an increase in the indications for genetic testing is expected.
dc.identifier.doi10.1159/000452280
dc.identifier.urihttps://doi.org/10.1159/000452280
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/51357
dc.language.isoen
dc.publisherKarger Publishers
dc.relation.ispartofOncology
dc.sourceHospital General Universitario Gregorio Marañón
dc.subjectMedicine
dc.subjectGenetic testing
dc.subjectInternal medicine
dc.subjectLynch syndrome
dc.subjectCancer
dc.subjectColorectal cancer
dc.subjectGastroenterology
dc.subjectOncology
dc.titleFive Years of Multidisciplinary Care in Hereditary Cancer: Our Experience in a Spanish University Hospital
dc.typearticle

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