Copy number variations identified in thyroid FNA specimens are associated with Hürthle cell cytomorphology
Author:
Affiliation:
1. Department of Pathology Yale University School of Medicine New Haven Connecticut
Publisher
Wiley
Subject
Cancer Research,Oncology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cncy.22569
Reference35 articles.
1. Impact of the Multi-Gene ThyroSeq Next-Generation Sequencing Assay on Cancer Diagnosis in Thyroid Nodules with Atypia of Undetermined Significance/Follicular Lesion of Undetermined Significance Cytology
2. Performance of a Multigene Genomic Classifier in Thyroid Nodules With Indeterminate Cytology
3. Analytical performance of the ThyroSeq v3 genomic classifier for cancer diagnosis in thyroid nodules
4. Copy Number Variation
5. Tumor Genotype Determines Phenotype and Disease-related Outcomes in Thyroid Cancer
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4. “Copy number alteration” as the sole molecular finding of a Thyroseq test is more commonly seen in Hurthle cell neoplasms;Diagnostic Cytopathology;2023-08-02
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