Vol. 14 No. 2 (2013) | Egyptian Journal of Medical Human Genetics

Review

Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service

Mohd Fareed, Mohammad Afzal

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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

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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

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Novel mutation predicted to disrupt SGOL1 protein function

Rohit Gupta, Mrinal Mishra, Prateek Tandon, Raunak Hisaria

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Consanguinity and its relevance to clinical genetics

Rabah M Shawky, Solaf M Elsayed, Mouchira E Zaki, Sahar M Nour El-Din, Ferihan M Kamal

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Analysis of aromatase (CYP19) gene in Iranian women with endometriosis

Hajar Saber, Zivar Salehi, Saiedeh Sadri

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Telomerase activity and apoptosis genes as parameters of lymphocyte aging in Down syndrome patients

Ekram Abdel-Salam, Iman Abdel-Meguid, Soheir Korraa

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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

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Efficacy of adhesive taping in controlling genu recurvatum in diplegic children: A pilot study

Asmaa M Ghalwash, Shorouk AW El-Shennawy, Manal S Abd-Elwahab

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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

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Helium Neon laser therapy for post mastectomy lymphedema and shoulder mobility

Mohamed M Khalaf, Maha A Hassan, Maha A Hassan, Zizi M Ibrahim, Zizi M Ibrahim

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Case Report

Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome

Hoda Tomoum, Solaf M Elsayed, Elizabeth Berry-Kravis

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Letter to the editor: Controversial report on sickle cell trait in Manipur, India

Maishnam Rustam Singh

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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

Mohammad Saad Zaghloul Salem

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 14 No. 2 (2013) / Articles

Articles

Review

Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service

Computational evaluation of small molecule inhibitors of RGS4 to regulate the dopaminergic control of striatal LTD

Association between the polymorphisms of matrix metalloproteinases 9 and 3 genes and risk of myocardial infarction in Egyptian patients

Novel mutation predicted to disrupt SGOL1 protein function

Consanguinity and its relevance to clinical genetics

Analysis of aromatase (CYP19) gene in Iranian women with endometriosis

Telomerase activity and apoptosis genes as parameters of lymphocyte aging in Down syndrome patients

Clinical characteristics and analysis of HFE gene variants (C282Y and H63D) in Jordanian Arab patients with age-related macular degeneration

Efficacy of adhesive taping in controlling genu recurvatum in diplegic children: A pilot study

Evaluation of micronucleus frequency by acridine orange fluorescent staining in bucccal epithelial cells of oral submucosus fibrosis (OSMF) patients

Helium Neon laser therapy for post mastectomy lymphedema and shoulder mobility

Case Report

Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome

Letter to the editor: Controversial report on sickle cell trait in Manipur, India

Reply to Letter to the Editor

Gene frequency of sickle cell trait among Muslim populations in a malarial belt of India, i.e., Manipur

Educational corner of the issue

Basic concepts of medical genetics, pathogenetics, part 3

Journal Identifiers