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Molecular Variants and Their Risks for Malignancy in Cytologically Indeterminate Thyroid Nodules
Background: Gene panels are routinely used to assess predisposition to hereditary cancers by simultaneously testing multiple susceptibility genes and/or variants. More recently, genetic panels have been implemented as part of solid tumor malignancy testing assessing somatic alterations. One example...
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| Publicat a: | Thyroid |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Mary Ann Liebert, Inc., publishers
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6864764/ https://ncbi.nlm.nih.gov/pubmed/31469053 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2019.0278 |
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