Accessing genetic variation: genotyping single nucleotide polymorphisms
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics,Molecular Biology
Link
http://www.nature.com/articles/35103535.pdf
Reference138 articles.
1. Sachidanandam, R. et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409, 928–933 (2001).
2. Venter, J. C. et al. The sequence of the human genome. Science 291, 1304–1351 (2001).References 1 and 2 report the frequency, distribution and features of single nucleotide variation from a whole-genome perspective, based on the results from the Human Genome Project and from Celera Genomics.
3. Evans, W. E. & Relling, M. V. Pharmacogenomics: translating functional genomics into rational therapeutics. Science 286, 487–491 (1999).
4. Davignon, J., Gregg, R. E. & Sing, C. F. Apolipoprotein E polymorphism and atherosclerosis. Arteriosclerosis 8, 1–21 (1988).
5. Bertina, R. M. et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369, 64–67 (1994).
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