Egyptian Journal of
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| Contents: April 2013 (Volume 14, Number 2) |
Editorial Board
Pages iii-iv
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Review Article
Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service
Mohd Fareed, Mohammad Afzal
[Abstract] [Full text]
Original Articles
Computational evaluation of small molecule inhibitors of RGS4 to regulate the dopaminergic control of striatal LTD
Krutika Satish Gaonkar, Gavish Gulati, K. Balu, Rituraj Purohit
[Abstract] [Full text]
Association between the polymorphisms of matrix metalloproteinases 9 and 3 genes and risk of myocardial infarction in Egyptian patients
Nadia I Sewelam, Eman R. Radwan, Ashraf W Andraos, Baher E Ibrahim, Manal M. Wilson
[Abstract] [Full text]
Novel mutation predicted to disrupt SGOL1 protein function
Rohit Gupta, Mrinal Mishra, Prateek Tandon, Raunak Hisaria
[Abstract]
[Full text]
Consanguinity and its relevance to clinical genetics
Rabah M. Shawky, Solaf M. Elsayed, Mouchira E. Zaki, Sahar M. Nour El-Din, Ferihan M. Kamal
[Abstract] [Full text]
Analysis of aromatase (CYP19) gene in Iranian women with endometriosis
Hajar Saber, Zivar Salehi, Saiedeh Sadri
[Abstract] [Full text]
Telomerase activity and apoptosis genes as parameters of lymphocyte aging in Down syndrome patients
Ekram Abdel-Salam, Iman Abdel-Meguid, Soheir Korraa
[Abstract] [Full text]
Clinical characteristics and analysis of HFE gene variants (C282Y and H63D) in Jordanian Arab patients with age-related macular degeneration
Asem Alkhateeb, Shadi Al-khatib, Ahmed Elbetieha, Tasnim Al-Rashaideh
[Abstract] [Full text]
Efficacy of adhesive taping in controlling genu recurvatum in diplegic children: A pilot study
Asmaa M. Ghalwash, Shorouk A.W. El-Shennawy, Manal S. Abd-Elwahab
[Abstract] [Full text]
Evaluation of micronucleus frequency by acridine orange fluorescent staining in bucccal epithelial cells of oral submucosus fibrosis (OSMF) patients
Smita Jyoti, Saif Khan, Mohammad Afzal, Falaq Naz, Yasir Hasan Siddique
[Abstract] [Full text]
Helium Neon laser therapy for post mastectomy lymphedema and shoulder mobility
Mohamed M. Khalaf, Maha A. Hassan, Zizi M. Ibrahim
[Abstract] [Full text]
Case Report
Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome
Hoda Tomoum, Solaf M. Elsayed, Elizabeth Berry-Kravis
[Abstract] [Full text]
Letters to the Editor
Letter to the editor: Controversial report on sickle cell trait in Manipur, India
Maishnam Rustam Singh
[Abstract] [Full
text]
Gene frequency of sickle cell trait among Muslim populations in a Malarial belt of India, i.e., Manipur
Ahsana Shah, Ruqaiya Hussain, Mohd Fareed, Mohammad Afzal
[Abstract] [Full
text]
EDUCATIONAL CORNER
Basic concepts of medical genetics, pathogenetics, part 3
Mohammad Saad Zaghloul Salem
[Abstract] [Full text]