Real-Time Polymerase Chain Reaction With Fluorescent Hybridization Probes for the Detection of Prevalent Mutations Causing Common Thrombophilic and Iron Overload Phenotypes-Reference-Cited by-同舟云学术

Real-Time Polymerase Chain Reaction With Fluorescent Hybridization Probes for the Detection of Prevalent Mutations Causing Common Thrombophilic and Iron Overload Phenotypes

Published:2001-03 Issue:3 Volume:115 Page:439-447
ISSN:0002-9173
Container-title:American Journal of Clinical Pathology
language:en
Short-container-title:Am J Clin Pathol

Author:

Parks Sharie B.,Popovich Bradley W.,Press Richard D.

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Link

http://academic.oup.com/ajcp/article-pdf/115/3/439/4983905/ajcpath115-0439.pdf

Reference27 articles.

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2. Miletich JP. Thrombophilia as a multigenic disorder. Semin Thromb Hemost. 1998;24(suppl 1):13-20.

3. Ridker PM, Hennekens CH, Lindpaintner K, et al. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. N Engl J Med. 1995;332:912-917.

4. Ridker PM, Miletich JP, Stampfer MJ, et al. Factor V Leiden and risks of recurrent idiopathic venous thromboembolism. Circulation. 1995;92:2800-2802.

5. Press RD. Hereditary hemochromatosis: impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease. Arch Pathol Lab Med. 1999;123:1053-1059.

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