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Germline mutations as potential causes of childhood solid tumours: comments on the Norwegian childhood cancer cohort study
Some cancer predisposing germline mutations cause overt birth defects and congenital anomalies. Others are clinically silent and can only be suspected by the presence of increased cancer incidence in family members. A new study shows that long-term monitoring of families may be needed to discover pr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931095/ https://www.ncbi.nlm.nih.gov/pubmed/29593336 http://dx.doi.org/10.1038/s41416-018-0059-0 |