Variations on a Theme: Cataloging Human DNA Sequence Variation-Reference-Cited by-同舟云学术

Variations on a Theme: Cataloging Human DNA Sequence Variation

Published:1997-11-28 Issue:5343 Volume:278 Page:1580-1581
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Collins Francis S.¹,Guyer Mark S.¹,Chakravarti Aravinda²

Affiliation:

1. F. S. Collins and M. S. Guyer are at the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-2152, USA. Collins. Guyer.

2. A. Chakravarti is in the Department of Genetics, Center for Human Genetics, Case Western Reserve University, Cleveland, OH 44106, USA.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference26 articles.

1. Collins F. S., Nature Genet.1, 3 (1992);

2. Ballabio A., ibid. 3, 277 (1993);

3. Collins F. S., ibid. 9, 347 (1995).

4. Prominent successes of this approach include the BRCA1 [Y. Miki et al. Science 266 66 (1994)] and BRCA2 [Wooster et al. Nature 378 789 (1995)] genes for breast and ovarian cancer

5. the DNA mismatch repair genes for hereditary nonpolyposis colon cancer (HNPCC) [C.E. Bronner et al. Nature 368 258 (1994)

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