Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 19 No. 1 (2018) / Articles

Published: 2018-03-13

Common variant of 5,10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population

Marzieh Attar, Seyedpayam Shirangi, Farnoosh Shateri, Majid Shahbazi

1–5

DOI:

10.1016/j.ejmhg.2017.11.004

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Abnormal maternal biomarkers of homocysteine and methionine metabolism and the risk of congenital heart defects

Rabah M. Shawky, Ahmed R.M. Ramy, Sahar M. Nour El-Din, Sawsan M. Abd Elmonem, Marwa A. Abd Elmonem

7–12

DOI:

10.1016/j.ejmhg.2017.08.004

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Association between Interleukin-18 promoter polymorphisms and risk of ischemic stroke: A case-control study

Noha M. Bakr, Noha A. Hashim, Ashraf Awad, Abdallah-Almamun Sarhan

13–18

DOI:

10.1016/j.ejmhg.2017.08.014

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The relation of thrombomodulin G33A and C1418T gene polymorphisms to the risk of acute myocardial infarction in Egyptians

Wael Alkhiary, Mohamed Abdalaal, Amr Mohamed El-Saddik

19–22

DOI:

10.1016/j.ejmhg.2017.08.007

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An association between apo-A4 gene polymorphism (Thr347Ser and Gln360His) and coronary artery disease in northern India

Pramod Kumar, Arbind Kumar Choudhary, Nibhriti Das

23–29

DOI:

10.1016/j.ejmhg.2017.07.001

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Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran

Seyedeh Zahra Mousavi, Aref Salehi, Eisa Jorjani, Reza Salehi Manzari, Touraj Farazmandfar, Majid Shahbazi

31–35

DOI:

10.1016/j.ejmhg.2017.06.005

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Prevalence of congenital heart defects among 54 Egyptian children with Maple syrup urine disease

Alyaa A. Kotby, Marwa M. Al-Fahham, Heba Salah A. Elabd, Osama K. Zaki

37–41

DOI:

10.1016/j.ejmhg.2017.10.001

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Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations

Behdokht Fathi Dizaji, Mahdi Rivandi, Ali Javandoost, Maryam Saberi Karimian, Atena Raei, Amirhossein Sahebkar, Gordon Ferns, Majid Ghayour Mobarhan, Alireza Pasdar

43–48

DOI:

10.1016/j.ejmhg.2017.12.001

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Cardiomyopathy in Vici syndrome

Rabah M. Shawky

49–50

DOI:

10.1016/j.ejmhg.2017.12.003

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Progress in genetics of coronary artery disease

Rabah M. Shawky

51–52

DOI:

10.1016/j.ejmhg.2017.11.001

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Journal Identifiers

eISSN: 1110-8630