Linkage disequilibrium across the fibrinogen locus as shown by five genetic polymorphisms, G/A−455 (HaeIII), C/T−148 (HindIII/AluI), T/G+1689 (AvaII), andBclI (β-fibrinogen) andTaqI (α-fibrinogen), and their detection by PCR-Reference-Cited by-同舟云学术

Linkage disequilibrium across the fibrinogen locus as shown by five genetic polymorphisms, G/A−455 (HaeIII), C/T−148 (HindIII/AluI), T/G+1689 (AvaII), andBclI (β-fibrinogen) andTaqI (α-fibrinogen), and their detection by PCR

Published:1994 Issue:1 Volume:3 Page:79-81
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Thomas Angela,Lamlum Hanan,Humphries Steve,Green Fiona

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Nucleotide Sequences of the Three Genes Coding for Human Fibrinogen

2. The role of fibrinogen as a cardiovascular risk factor

3. Fibrinogen genotype and risk of peripheral atherosclerosis

4. (1993) The role of β-fibrinogen genotype in determining plasma fibrinogen levels in young survivors of myocardial infarction and healthy controls from Sweden. Thromb Haemostas (in press).

5. The identification of a DNA polymorphism of the ? fibrinogen gene, and the regional assignment of the human fibrinogen genes to 4q26-qter

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