This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Functional annotation of variants of the BRCA2 gene via locally haploid human pluripotent stem cells
Nature Biomedical Engineering Open Access 24 July 2023
-
Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context
Scientific Reports Open Access 12 October 2015
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Jensen, R.A. et al. Nature Genet. 12, 303–308 (1996).
Wooster, R. et al. Nature 378, 789–792 (1995).
Tavtigian, S.V. et al. Nature Genet. 12, 333–337 (1996).
Teng, D.H-F. et al. Nature Genet. 13, 241–244 (1996).
Couch, F.J. et al. Nature Genet. 13, 123–125 (1996).
Friend, S. et al. Nature Genet. 11, 238–239 (1995).
Riboli, E. et al. Ann. Oncol. 3, 783–791 (1992).
Dunning, A.M. et al. Am. J. Hum. Genet. 50, 208–221 (1992).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Mazoyer, S., Dunning, A., Serova, O. et al. A polymorphic stop codon in BRCA2. Nat Genet 14, 253–254 (1996). https://doi.org/10.1038/ng1196-253
Issue Date:
DOI: https://doi.org/10.1038/ng1196-253
This article is cited by
-
Functional annotation of variants of the BRCA2 gene via locally haploid human pluripotent stem cells
Nature Biomedical Engineering (2023)
-
Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal
Journal of Human Genetics (2016)
-
Evidence for a pathogenic role of BRCA1 L1705P and W1837X germ-line mutations
Molecular Biology Reports (2016)
-
Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context
Scientific Reports (2015)
-
Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes
Breast Cancer Research and Treatment (2014)