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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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| Vydáno v: | Thyroid |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Mary Ann Liebert, Inc., publishers
2019
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| Témata: | |
| On-line přístup: | 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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