This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
TP53 mutations in ovarian carcinomas from sporadic cases and carriers of two distinct BRCA1 founder mutations; relation to age at diagnosis and survival
BMC Cancer Open Access 17 October 2005
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
Motulsky, A.G. Nature Genet. 9, 99–101 (1995).
Struewing, J.P. et al. Nature Genet. 11, 198–200 (1995).
Shattuck-Eidens, D. et al. J. Am. med. Assoc. 273, 535–541 (1995).
Tonin, P. et al. Am. J. hum. Genet. 57, 189 (1995).
Struewing, J.P. et al. Am. J. hum. Genet. 57, 1–7 (1995).
Ford, D. et al. Am. J. hum. Genet. (in the press).
Risch, N. et al. Nature Genet. 9, 152–159 (1995).
Zoossmann-Diskin, A. Nature Genet. 11, 13–14 (1995).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Goldgar, D., Reilly, P. A common BRCA1 mutation in the Ashkenazim. Nat Genet 11, 113–114 (1995). https://doi.org/10.1038/ng1095-113
Issue Date:
DOI: https://doi.org/10.1038/ng1095-113
This article is cited by
-
TP53 mutations in ovarian carcinomas from sporadic cases and carriers of two distinct BRCA1 founder mutations; relation to age at diagnosis and survival
BMC Cancer (2005)
-
Abschätzung des Krebsrisikos durch genetische Analyse?
Strahlentherapie und Onkologie (1997)