Register for email alerts and news feeds:
This journal | BMJ Group
rss
Journal of Medical Genetics 1999;36:720-721; doi:10.1136/jmg.36.9.720
Copyright © 1999 by the BMJ Publishing Group Ltd.
J Med Genet 1999;36:720-721 ( September )

Letters to the editor

Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer

The first 150 words of the full text of this article appear below.

EDITOR---A number of genes are now known to be involved in inherited susceptibility to breast cancer. In the context of multiple case families, the most well identified and characterised genes are BRCA1 on 17q1 2 and BRCA2 on 13q.3 4 Both linkage and mutation studies indicate that these genes account for the large majority of families segregating both early age of onset breast cancer and ovarian cancer, and those with both male and female breast cancer cases. However, other studies5-8 indicate that BRCA1 and BRCA2 account for less than half of site specific breast cancer families, suggesting that other major susceptibility genes may be important in this group. We therefore initiated a collaborative genomic search, using a large panel of female breast cancer only families in which germline mutations in the BRCA1 and BRCA2 coding sequence were not detected and in which there was no strong evidence of linkage to . . . [Full text of this article]


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Nathanson, K. L., Shugart, Y. Y., Omaruddin, R., Szabo, C., Goldgar, D., Rebbeck, T. R., Weber, B. L. (2002). CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q. Hum Mol Genet 11: 1327-1332 [Abstract] [Full Text]  
  • Thompson, D., Szabo, C. I., Mangion, J., Oldenburg, R. A., Odefrey, F., Seal, S., Barfoot, R., Kroeze-Jansema, K., Teare, D., Rahman, N., Renard, H., KConFab Consortium, , Mann, G., Hopper, J. L., Buys, S. S., Andrulis, I. L., Senie, R., Daly, M. B., West, D., Ostrander, E. A., Offit, K., Peretz, T., Osorio, A., Benitez, J., Nathanson, K. L., Sinilnikova, O. M., Olah, E., Bignon, Y.-J., Ruiz, P., Badzioch, M. D., Vasen, H. F. A., Futreal, A. P., Phelan, C. M., Narod, S. A., Lynch, H. T., Ponder, B. A. J., Eeles, R. A., Meijers-Heijboer, H., Stoppa-Lyonnet, D., Couch, F. J., Eccles, D. M., Evans, D. G., Chang-Claude, J., Lenoir, G., Weber, B. L., Devilee, P., Easton, D. F., Goldgar, D. E., Stratton, M. R. (2002). From the Cover: Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium. Proc. Natl. Acad. Sci. USA 99: 827-831 [Abstract] [Full Text]  
  • Nathanson, K. L., Weber, B. L. (2001). 'Other' breast cancer susceptibility genes: searching for more holy grail. Hum Mol Genet 10: 715-720 [Abstract] [Full Text]  
  • Thompson, D., Szabo, C. I., Mangion, J., Oldenburg, R. A., Odefrey, F., Seal, S., Barfoot, R., Kroeze-Jansema, K., Teare, D., Rahman, N., Renard, H., KConFab Consortium, , Mann, G., Hopper, J. L., Buys, S. S., Andrulis, I. L., Senie, R., Daly, M. B., West, D., Ostrander, E. A., Offit, K., Peretz, T., Osorio, A., Benitez, J., Nathanson, K. L., Sinilnikova, O. M., Olah, E., Bignon, Y.-J., Ruiz, P., Badzioch, M. D., Vasen, H. F. A., Futreal, A. P., Phelan, C. M., Narod, S. A., Lynch, H. T., Ponder, B. A. J., Eeles, R. A., Meijers-Heijboer, H., Stoppa-Lyonnet, D., Couch, F. J., Eccles, D. M., Evans, D. G., Chang-Claude, J., Lenoir, G., Weber, B. L., Devilee, P., Easton, D. F., Goldgar, D. E., Stratton, M. R. (2002). From the Cover: Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium. Proc. Natl. Acad. Sci. USA 99: 827-831 [Abstract] [Full Text]  

This Article

Services
Citing Articles
Google Scholar
PubMed
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Genetics jobs

Genetics jobs