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Identification of Lynch Syndrome in Patients with Endometrial Cancer Based on a Germline Next Generation Sequencing Multigene Panel Test
SIMPLE SUMMARY: Lynch Syndrome (LS) is a hereditary cancer syndrome caused by an autosomal dominant mutation in one of the DNA mismatch repair (MMR) genes. Understanding the clinical traits of endometrial cancer, which is one of the most frequent as well as the earliest diagnosed cancer types of LS-...
Autores principales: | Kim, Yoo-Na, Kim, Min Kyu, Lee, Young Joo, Lee, Youngeun, Sohn, Ji Yeon, Lee, Jung-Yun, Choi, Min Chul, Kim, Migang, Jung, Sang Geun, Joo, Won Duk, Lee, Chan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316192/ https://www.ncbi.nlm.nih.gov/pubmed/35884469 http://dx.doi.org/10.3390/cancers14143406 |
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