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Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis
Multiple primary cancers, defined as three or more primary tumours, are rare, and there are few genetic studies concerning them. There is a need for increased knowledge on the heritability of multiple primary cancers and genotype-phenotype correlations. We have performed whole-genome/exome sequencin...
Autores principales: | Wallander, Karin, Thonberg, Håkan, Nilsson, Daniel, Tham, Emma |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555269/ https://www.ncbi.nlm.nih.gov/pubmed/34711244 http://dx.doi.org/10.1186/s13053-021-00203-z |
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