Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Jan 9:2021:6611963.
doi: 10.1155/2021/6611963. eCollection 2021.

Should All Individuals Be Screened for Genetic Predisposition to Cancer?

Sarah Wedderburn  1 , Terri P McVeigh  2
Affiliations
Review

Should All Individuals Be Screened for Genetic Predisposition to Cancer?

Sarah Wedderburn et al. Genet Res (Camb). .
No abstract available

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Similar articles

See all similar articles

Cited by

References

    1. Wilson J. M. G., Jungner G. Principles and Practice of Screening for Disease. Geneva, Switzerland: World Health Organization; 1968. - PubMed
    1. Auton A., Auton A., Brooks L. D., et al. A global reference for human genetic variation. Nature. 2015;526(7571):68–74. doi: 10.1038/nature15393. - DOI - PMC - PubMed
    1. Pinto D., Pinto C., Guerra J., et al. Contribution of MLH1 constitutional methylation for Lynch syndrome diagnosis in patients with tumor MLH1 downregulation. Cancer Medicine. 2018;7(2):p. 433. doi: 10.1002/cam4.1285. - DOI - PMC - PubMed
    1. Mussa A., Molinatto C., Baldassarre G., et al. Cancer risk in Beckwith-Wiedemann syndrome: a systematic review and meta-analysis outlining a novel (Epi)Genotype specific histotype targeted screening protocol. The Journal of Pediatrics. 2016;176:142–149. doi: 10.1016/j.jpeds.2016.05.038. - DOI - PubMed
    1. Morak M., Steinke-Lange V., Massdorf T., et al. Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics. Familial Cancer. 2020;19(2):p. 161. doi: 10.1007/s10689-020-00159-4. - DOI - PubMed

LinkOut - more resources