Progress in genetics of coronary artery disease.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 51, doi. 10.1016/j.ejmhg.2017.11.001
- By:
- Publication type:
- Article
Works matching IS 1110-8630 AND VI 19 AND IP 1 AND DT 2018
Results: 10
1
2
Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 31, doi. 10.1016/j.ejmhg.2017.06.005
- By:
- Publication type:
- Article
3
Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 43, doi. 10.1016/j.ejmhg.2017.12.001
- By:
- Publication type:
- Article
4
An association between apo-A4 gene polymorphism (Thr347Ser and Gln360His) and coronary artery disease in northern India.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 23, doi. 10.1016/j.ejmhg.2017.07.001
- By:
- Publication type:
- Article
5
Common variant of 5,10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 1, doi. 10.1016/j.ejmhg.2017.11.004
- By:
- Publication type:
- Article
6
Cardiomyopathy in Vici syndrome.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
7
Association between Interleukin-18 promoter polymorphisms and risk of ischemic stroke: A case-control study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 13, doi. 10.1016/j.ejmhg.2017.08.014
- By:
- Publication type:
- Article
8
The relation of thrombomodulin G33A and C1418T gene polymorphisms to the risk of acute myocardial infarction in Egyptians.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 19, doi. 10.1016/j.ejmhg.2017.08.007
- By:
- Publication type:
- Article
9
Prevalence of congenital heart defects among 54 Egyptian children with Maple syrup urine disease.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 37, doi. 10.1016/j.ejmhg.2017.10.001
- By:
- Publication type:
- Article
10
Abnormal maternal biomarkers of homocysteine and methionine metabolism and the risk of congenital heart defects.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 1, p. 7, doi. 10.1016/j.ejmhg.2017.08.004
- By:
- Publication type:
- Article