Skip Navigation

JNCI Journal of the National Cancer Institute 2006 98(3):162; doi:10.1093/jnci/djj062
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (1)
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Vastag, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vastag, B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© Oxford University Press 2006.

NEWS

NIH Institutes Launch Joint Venture To Map Cancer Genome

Brian Vastag

The first 10% of the full text of this article appears below.

In December, National Institutes of Health leaders announced plans for a pilot program that they hope will map every genetic mutation involved in cancer. Francis Collins, M.D., Ph.D., director of the National Human Genome Research Institute, said that the effort, called the Cancer . . . [Full Text of this Article]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
F. Dahl, J. Stenberg, S. Fredriksson, K. Welch, M. Zhang, M. Nilsson, D. Bicknell, W. F. Bodmer, R. W. Davis, and H. Ji
Multigene amplification and massively parallel sequencing for cancer mutation discovery
PNAS, May 29, 2007; 104(22): 9387 - 9392.
[Abstract] [Full Text] [PDF]