Genome association study of human chromosome 13 and susceptibility to coronary artery disease in a Chinese population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s12041-013-0207-5.pdf
Reference31 articles.
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2. Arking D. E., Becker D. M., Yanek L. R., Fallin D., Judge D. P., Moy T. F. et al. 2003 KLOTHO allele status and the risk of early-onset occult coronary artery disease. Am. J. Hum. Genet. 72, 1154–1161.
3. Assimes T. L., Knowles J. W., Priest J. R., Basu A., Volcik K. A. Southwick A. et al. 2008 Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease. Hum. Genet. 123, 399–408.
4. Barcellos L. F., Klitz W., Field L. L., Tobias R., Bowcock A. M., Wilson R. et al. 1997 Association mapping of disease loci, by use of a pooled DNA genomic screen. Am. J. Hum. Genet. 61, 734–747.
5. Beanlands R. S., Chow B. J., Dick A., Friedrich M. G., Gulenchyn K. Y., Kiess M. et al. 2007 CCS/CAR/CANM/CNCS/ CanSCMR joint position statement on advanced noninvasive cardiac imaging using position emission tomography, magnetic resonance imaging and multidetector computed tomographic angiography in the diagnosis and evaluation of ischemic heart disease-executive summary. Can. J. Cardiol. 23, 107–119.
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