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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...

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Detalles Bibliográficos
Autores principales: Ravindranath, Yaddanapudi, Spector, Logan G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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