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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
Autors principals: Goldner, Whitney S., Angell, Trevor E., McAdoo, Sallie Lou, Babiarz, Joshua, Sadow, Peter M., Nabhan, Fadi A., Nasr, Christian, Kloos, Richard T.
Format: Artigo
Idioma:Inglês
Publicat: Mary Ann Liebert, Inc., publishers 2019
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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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