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Egyptian Journal of Medical Human Genetics - Vol 14, No 2 (2013)

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Table of Contents

Articles

Review

Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service
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Mohd Fareed, Mohammad Afzal
Computational evaluation of small molecule inhibitors of RGS4 to regulate the dopaminergic control of striatal LTD EMAIL FREE FULL TEXT
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Krutika Satish Gaonkar, Gavish Gulati, K Balu, Rituraj Purohit
Association between the polymorphisms of matrix metalloproteinases 9 and 3 genes and risk of myocardial infarction in Egyptian patients EMAIL FREE FULL TEXT
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Nadia I Sewelam, Eman R Radwan, Ashraf W Andraos, Baher E Ibrahim, Manal M Wilson
Novel mutation predicted to disrupt SGOL1 protein function EMAIL FREE FULL TEXT
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Rohit Gupta, Mrinal Mishra, Prateek Tandon, Raunak Hisaria
Consanguinity and its relevance to clinical genetics EMAIL FREE FULL TEXT
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Rabah M Shawky, Solaf M Elsayed, Mouchira E Zaki, Sahar M Nour El-Din, Ferihan M Kamal
Analysis of aromatase (CYP19) gene in Iranian women with endometriosis EMAIL FREE FULL TEXT
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Hajar Saber, Zivar Salehi, Saiedeh Sadri
Telomerase activity and apoptosis genes as parameters of lymphocyte aging in Down syndrome patients EMAIL FREE FULL TEXT
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Ekram Abdel-Salam, Iman Abdel-Meguid, Soheir Korraa
Clinical characteristics and analysis of HFE gene variants (C282Y and H63D) in Jordanian Arab patients with age-related macular degeneration EMAIL FREE FULL TEXT
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Asem Alkhateeb, Shadi Al-khatib, Ahmed Elbetieha, Tasnim Al-Rashaideh
Efficacy of adhesive taping in controlling genu recurvatum in diplegic children: A pilot study EMAIL FREE FULL TEXT
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Asmaa M Ghalwash, Shorouk AW El-Shennawy, Manal S Abd-Elwahab
Evaluation of micronucleus frequency by acridine orange fluorescent staining in bucccal epithelial cells of oral submucosus fibrosis (OSMF) patients EMAIL FREE FULL TEXT
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Smita Jyoti, Saif Khan, Mohammad Afzal, Falaq Naz, Yasir Hasan Siddique
Helium Neon laser therapy for post mastectomy lymphedema and shoulder mobility EMAIL FREE FULL TEXT
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Mohamed M Khalaf, Maha A Hassan, Maha A Hassan, Zizi M Ibrahim, Zizi M Ibrahim
Case Report

Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome
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Hoda Tomoum, Solaf M Elsayed, Elizabeth Berry-Kravis
Letter to the editor: Controversial report on sickle cell trait in Manipur, India EMAIL FREE FULL TEXT
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Maishnam Rustam Singh
Reply to Letter to the Editor

Gene frequency of sickle cell trait among Muslim populations in a malarial belt of India, i.e., Manipur
A Shah, R Hussain, M Fareed, M Afzal
Educational corner of the issue

Basic concepts of medical genetics, pathogenetics, part 3
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Mohammad Saad Zaghloul Salem


The Egyptian Journal Of Medical Human Genetics.   ISSN: 1110-8630