Copy number variations: A novel molecular marker for papillary thyroid cancer

BACKGROUND: We aimed to screen tumor-associated functional genes on a large scale through copy number variation (CNV) analysis of papillary thyroid cancer (PTC). METHODS: We analyzed 74 tissue samples from 41 patients with thyroid nodules. The samples were subjected to whole-genome resequencing and...

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Detalles Bibliográficos
Autores principales: Lai, Xingjian, Gao, Luying, Zhou, Gaoying, Xu, Xiequn, Wang, Jinhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589167/
https://www.ncbi.nlm.nih.gov/pubmed/36299525
http://dx.doi.org/10.1016/j.heliyon.2022.e11107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589167/
https://www.ncbi.nlm.nih.gov/pubmed/36299525
http://dx.doi.org/10.1016/j.heliyon.2022.e11107

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