Vol. 16 No. 3 (2015) | Egyptian Journal of Medical Human Genetics

Review: Cytokines in Gaucher disease: Role in the pathogenesis of bone and pulmonary disease

AAG Tantawy

207-213

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Allelic prevalence of intron 3 insertion/deletion genetic polymorphism of DNA double-strand break repair gene XRCC4 in four healthy Iranian populations

L Fallahzadeh-Abarghooei, T Zahedi, F Mirabedi, M Saadat

215-218

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Association of CYP3A4 and CYP3A5 polymorphisms with Iranian breast cancer patients

E Badavi, B Safavi, A Jalali, GM Shahriary, J Mohammadi-Asl, J Babaei

219-225

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Lower HOMA-β values are detected among individuals with variant of E23K polymorphism of potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) gene

R Sunita, AH Sadewa, A Farmawati

227-231

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Contrasting genetic influence of PON 1 coding gene polymorphisms L55M and Q192R on individuals’ response to environmental agents

NYS Morcos, MK El-Masry, MM Kamal, SY Galal

233-237

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Occurrence and detection of AmpC β-lactamases among Enterobacteriaceae isolates from patients at Ain Shams University Hospital

SA El-Hady, LA Adel

239-244

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Molecular study of developmental sex disorders in children

SS AboElella, MAM Tawfik, WMM Abo El-Fotoh

245-256

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Assessment of the efficacy of desmopressin in treatment of Primary Monosymptomatic Nocturnal Enuresis in Egyptian children

F ElBaz, S Zahra, M Khairy

257-262

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Sarcopenic obesity and dyslipidemia response to selective exercise program after liver transplantation

MA Basha, ZE Mowafy, EA Morsy

263-268

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Shock wave therapy for spastic plantar flexor muscles in hemiplegic cerebral palsy children

HAA Gawad, AH Mohammed, AEA Karim

269-275

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 16 No. 3 (2015) / Articles

Articles

Review: Cytokines in Gaucher disease: Role in the pathogenesis of bone and pulmonary disease

Allelic prevalence of intron 3 insertion/deletion genetic polymorphism of DNA double-strand break repair gene XRCC4 in four healthy Iranian populations

Association of CYP3A4 and CYP3A5 polymorphisms with Iranian breast cancer patients

Lower HOMA-β values are detected among individuals with variant of E23K polymorphism of potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) gene

Contrasting genetic influence of PON 1 coding gene polymorphisms L55M and Q192R on individuals’ response to environmental agents

Occurrence and detection of AmpC β-lactamases among Enterobacteriaceae isolates from patients at Ain Shams University Hospital

Molecular study of developmental sex disorders in children

Assessment of the efficacy of desmopressin in treatment of Primary Monosymptomatic Nocturnal Enuresis in Egyptian children

Sarcopenic obesity and dyslipidemia response to selective exercise program after liver transplantation

Shock wave therapy for spastic plantar flexor muscles in hemiplegic cerebral palsy children

CASE REPORT Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child

Plummer Vinson syndrome in a male and his chromosomal study – A case report

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