Vol. 18 No. 4 (2017) | Egyptian Journal of Medical Human Genetics

Ahmed El-Shenawy, Manal Diab, Mohamed Shemis, Maged El-Ghannam, Dalia Salem, Moustafa Abdelnasser, Mohamed Shahin, Mahmoud Abdel-Hady, Effat El-Sherbini, Mohamed Saber

365–371

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Role of toll like receptors in bacterial and viral diseases – A systemic approach

Avishek Das, Pokhraj Guha, Debapriya Sen, Tapas Kumar Chaudhuri

373–379

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A comparative study of mutation screening of sarcomeric genes (MYBPC3, MYH7, TNNT2) using single gene approach versus targeted gene panel next generation sequencing in a cohort of HCM patients in Egypt

Heba Sh. Kassem, Roddy Walsh, Paul J. Barton, Besra S. Abdelghany, Remon S. Azer, Rachel Buchan, Shibu John, Ahmed Elguindy, Sarah Moharem-ElGamal, Hala M. Badran, Hoda Shehata, Stuart A. Cook, Magdi H. Yacoub

381–387

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Extremely low frequency electromagnetic field in combination with β-Lapachone up-regulates the genes of non-homologous end joining

Fatemeh Sanie-Jahromi, Hamideh Mahmoudinasab, Mostafa Saadat

389–392

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An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings

Solaf M. Elsayed, Radwa Gamal

393–396

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II

Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad

397-401

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 18 No. 4 (2017) / Articles

Articles

CYP2D6 pharmacogenomics

Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population

Identification of functional SNPs in human LGALS3 gene by in silico analyses

Germline variants in the ATM gene and breast cancer susceptibility in Moroccan women: A meta-analysis

Distribution of HLA-DRB1/DQB1 alleles and DRB1-DQB1 haplotypes among Tunisian patients with autoimmune hepatitis

Open-array analysis of genetic variants in Egyptian patients with type 2 diabetes and obesity

Screening of polymorphisms in the folate pathway in Turkish pediatric Acute Lymphoblastic Leukemia patients

Comparison of multiplex reverse transcription-PCR-enzyme hybridization assay with immunofluorescence techniques for the detection of four viral respiratory pathogens in pediatric community acquired pneumonia

Association assessment of platelet derived growth factor B gene polymorphism and its expression status with susceptibility to coronary artery disease

Detection of Helicobacter pylori vacA, cagA and iceA1 virulence genes associated with gastric diseases in Egyptian patients

Role of toll like receptors in bacterial and viral diseases – A systemic approach

A comparative study of mutation screening of sarcomeric genes (MYBPC3, MYH7, TNNT2) using single gene approach versus targeted gene panel next generation sequencing in a cohort of HCM patients in Egypt

Extremely low frequency electromagnetic field in combination with β-Lapachone up-regulates the genes of non-homologous end joining

An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II

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