Vol. 17 No. 2 (2016) | Egyptian Journal of Medical Human Genetics

Review: Natural killer cells enhance the immune surveillance of cancer

Faisal Nouroz, Farzana Bibi, Shumaila Noreen, Nosheen Masood

149-154

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Cytokine gene polymorphisms and their association with cervical cancer: A North Indian study

Maneesh Kumar Gupta, Renu Singh, Monisha Banerjee

155-163

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Molecular characterization of X chromosome fragility in idiopathic mental retardation

Heba Alla Hosny Omar, Tarek M. Kamal, Heba Salah Abd-Alkhalek, Ghada H. El Nady, MSZ Salem

165-172

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The association between (8390G>A) single nucleotide polymorphism in APOE gene with Alzheimer’s and Parkinson disease

Faranak Mohammadpour Lashkari, Anahita Mohseni Meybodi, Zahra Mansouri, Hamid Kalantari, Kamelia Farahmand, Hamidreza Vaziri

185-189

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Sirtuin 1 gene rs2273773 C >T single nucleotide polymorphism and protein oxidation markers in asthmatic patients

Aida Abdeen Mahmoud, Abdellah Hamed Khalil Ali, Essam Nour Eldin

191-196

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Cardiological assessment of a cohort of Egyptian patients with osteogenesis imperfecta type III

Heba Salah A. ElAbd, Mohamed Moghazy

197-200

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Inducible protective processes in animal systems XIV: Cytogenetic adaptive response induced by EMS or MMS in bone marrow cells of diabetic mouse

BB Dada Khalandar, V Vasudev

201-208

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Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML

Dilara Fatma Akin, Deniz Aslar Oner, Mine Mumcuoglu, Ustun Ezer, Muhterem Bahce, Emin Kurekci, Nejat Akar

209-215

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Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt

Maha Moustafa, Elham Gaber, Gamal Abo El Fath

217-221

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Partial association of restriction polymorphism of the ligand binding domain of human androgen receptor in prostate cancer

Mohamed Hessien, Ahmed El Barbary, Saad el Gendy, Amira Nabil

223-228

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Griscelli syndrome type 2 – A case report and clinical approach to silver blonde hair

Sana Durrani, Michael Chicka, Bushra Afroze

229-232

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Fraser syndrome: Phenotypic variability and unusual findings in four Egyptian families

Ebtesam M. Abdalla, Louay H. Zayed, Noha M. Issa, Asmaa K. Amin

233-238

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Corrigendum to ‘‘A novel nonsense mutation in the cathepsin C gene in an Egyptian patient presenting with Papillon–Lefe`vre syndrome” [Egypt. J. Med. Hum. Genet. 16 (4) (2015) 387–392]

Hala Soliman, Heba Gamal Eldeen, Mostafa Ibrahim Mostafa

239

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Role of MTHFR A1298C gene polymorphism in the etiology of prostate cancer: A systematic review and updated meta-analysis

U Yadav, P Kumar, V Rai

141-148

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 17 No. 2 (2016) / Articles

Articles

Review: Natural killer cells enhance the immune surveillance of cancer

Cytokine gene polymorphisms and their association with cervical cancer: A North Indian study

Molecular characterization of X chromosome fragility in idiopathic mental retardation

The association between (8390G>A) single nucleotide polymorphism in APOE gene with Alzheimer’s and Parkinson disease

Sirtuin 1 gene rs2273773 C >T single nucleotide polymorphism and protein oxidation markers in asthmatic patients

Cardiological assessment of a cohort of Egyptian patients with osteogenesis imperfecta type III

Inducible protective processes in animal systems XIV: Cytogenetic adaptive response induced by EMS or MMS in bone marrow cells of diabetic mouse

Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML

Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt

Partial association of restriction polymorphism of the ligand binding domain of human androgen receptor in prostate cancer

Griscelli syndrome type 2 – A case report and clinical approach to silver blonde hair

Fraser syndrome: Phenotypic variability and unusual findings in four Egyptian families

Corrigendum to ‘‘A novel nonsense mutation in the cathepsin C gene in an Egyptian patient presenting with Papillon–Lefe`vre syndrome” [Egypt. J. Med. Hum. Genet. 16 (4) (2015) 387–392]

Role of MTHFR A1298C gene polymorphism in the etiology of prostate cancer: A systematic review and updated meta-analysis

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