Vol. 19 No. 3 (2018) | Egyptian Journal of Medical Human Genetics

Zahra Malekshahi, Mahdi Mahmoudi, Massoomeh Akhlaghi, Masoud Garshasbi, Ahmadreza Jamshidi, Shiva Poursani, Shayan Mostafaei, Mohammad Hossein Nicknam

185–189

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Association of variable number tandem repeats polymorphism in the IL-4 gene with end-stage renal disease in children

Eman A. Elghoroury, Fatina I. Fadel, Hebatallah Farouk, Manal F. Elshamaa, Solaf Kamel, Dina Kandil, Eman Mahmoud

191–195

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Expression study of CYP19A1 gene in a cohort of Iranian leiomyoma patients

Leila Emrahi, Javad Behroozi, Shirin Shahbazi

197–200

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Association of proinflammatory cytokine IL-20 gene polymorphism with psoriasis in north Indian population

Aadil Wani, Bashir Ahmad Ganai, Tahseena Akhtar, Tarun Narang, Rajinder Kaur

201–205

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Copy number variation in VEGF gene as a biomarker of susceptibility to age-related macular degeneration

Norshakimah Md Bakri, Vasudevan Ramachandran, Hoo Fan Kee, Visvaraja Subrayan, Hazlita Isa, Nor Fariza Ngah, Nur Afiqah Mohamad, Ching Siew Mooi, Chan Yoke Mun, Patimah Ismail, Fazliana Ismail, Erma Suryana Sukiman, Wan Alia Wan Sulaiman

207–213

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Genotyping of PPAR-γ gene polymorphism in Egyptian neonates affected with sepsis disease and its severity

Rabah M. Shawky, Tarek M. Kamal, Shaimaa Raafat, Ghada H. El Nady

215–220

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A modified protocol for highly efficient EBV-mediated immortalization of human B lymphocytes from small volumes of peripheral blood serum

Natalya A. Lemskaya

221–223

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Risk factors of neural tube defects: A reality of Batna region in Algeria

Romyla Bourouba, Bakhouche Houcher, Nejat Akar

225–229

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Association of P2X7 gene common polymorphisms with pulmonary tuberculosis in Lur population of Iran

Ali Amiri, Toomaj Sabooteh, Seyyed Amir Yasin Ahmadi, Alireza Azargoon, Farhad Shahsavar

231–234

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Association of interleukin-6 and its -174G/C promoter polymorphism with clinical and laboratory characteristics of non hepatitis C virus rheumatoid arthritis patients

Reham Mohamed Raafat Hamed, Soliman Aref Mohamed, Reham Ali Dwedar, Yasmine Samy Elkholy, Fatema Talaat Elgengehy

235–240

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Association of nonalcoholic fatty liver disease grades with the plasma cell antigen-1 (PC-1) gene polymorphism

Ibrahim H. Borai, Yehia Mohamed Shaker, Maha Moustafa Kamal, Wafaa M. Ezzat, Esmat Ashour, Mie Afify, Weaam Gouda, Maha M. Elbrashy

241–246

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No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population

Azadeh Abtahi, Nader Mansour Samaei, Naghmeh Gholipour, Noorodin Moradi

247–251

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Yield of karyotyping in children with developmental delay and/or dysmorphic features in Sohag University Hospital, Upper Egypt

Abdelrahim A. Sadek, Mostafa Ashry Mohamed

253–259

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Association of toll-like receptor 2 polymorphisms with susceptibility to pulmonary tuberculosis in Sudanese

H. Zaki, N. Gasmelseed, B. Abdalla, S.P. Yip

261–265

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Evaluation of dysmorphic children according to echocardiographic findings: A single center experience

Muhsin Elmas, Ayhan Pektas, Mustafa Solak

267–270

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Case Report: A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia

Didem Torun Özkan, Nejat Akar

271–272

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 19 No. 3 (2018) / Articles

Articles

Review: Modified T-cells (using TCR and CTAs), chimeric antigen receptor (CAR) and other molecular tools in recent gene therapy

Review: Autism and KIR genes of the human genome: A brief meta-analysis

Review: Oncolytic virotherapy – A novel strategy for cancer therapy

Review: Determinants and modifiers of bleeding phenotypes in haemophilia-A: General and tropical perspectives

Impact of cell death pathway genes Fas 21377AA and FasL 2844CC polymorphisms on the risk of developing non-small cell lung cancer

Evaluation of the association of single nucleotide polymorphisms in DDP4 and CDK5RAP2 genes with rheumatoid arthritis susceptibility in Iranian population

Association of variable number tandem repeats polymorphism in the IL-4 gene with end-stage renal disease in children

Expression study of CYP19A1 gene in a cohort of Iranian leiomyoma patients

Association of proinflammatory cytokine IL-20 gene polymorphism with psoriasis in north Indian population

Copy number variation in VEGF gene as a biomarker of susceptibility to age-related macular degeneration

Genotyping of PPAR-γ gene polymorphism in Egyptian neonates affected with sepsis disease and its severity

A modified protocol for highly efficient EBV-mediated immortalization of human B lymphocytes from small volumes of peripheral blood serum

Risk factors of neural tube defects: A reality of Batna region in Algeria

Association of P2X7 gene common polymorphisms with pulmonary tuberculosis in Lur population of Iran

Association of interleukin-6 and its -174G/C promoter polymorphism with clinical and laboratory characteristics of non hepatitis C virus rheumatoid arthritis patients

Association of nonalcoholic fatty liver disease grades with the plasma cell antigen-1 (PC-1) gene polymorphism

No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population

Yield of karyotyping in children with developmental delay and/or dysmorphic features in Sohag University Hospital, Upper Egypt

Association of toll-like receptor 2 polymorphisms with susceptibility to pulmonary tuberculosis in Sudanese

Evaluation of dysmorphic children according to echocardiographic findings: A single center experience

Case Report: A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia

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