Vol. 18 No. 3 (2017) | Egyptian Journal of Medical Human Genetics

Tahia H. Saleem, Mohammed H. Hassan, Ahmed El-Abd Ahmed, Ayat A. Sayed, Nahed A. Mohamed, Khalid I. Elsayh, Abdallah M.A.A. El-Ebidi, Norhan B.B. Mohammed

249-255

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Prevalence of food addiction and its relationship to body mass index

Alaa Youssef Ahmed, Amany Mohammed Sayed

257-260

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Effect of ABCB1 (3435C>T) and CYP3A5 (6986A>G) genes polymorphism on tacrolimus concentrations and dosage requirements in liver transplant patients

Marwa Helal, Manar Obada, Wael Abd Elrazek, Manal Safan, Tarek Abd El-Hakim, Hala El-Said

261-268

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Vitamin D status, receptor gene BsmI (A/G) polymorphism and breast cancer in a group of Egyptian females

Rasha Rizk Elzehery, Azza A. Baiomy, Mohamed AbdEl-Fattah Hegazy, Rami Fares, Abdel-Hady El-Gilany, Refaat Hegazi

269-273

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Contribution of coagulation factor VII R353Q polymorphism to the risk of thrombotic disorders development (venous and arterial): A case-control study

Hanan Azzam, Reham M. El-Farahaty, Nashwa K. Abousamra, Hossam Elwakeel, Sherif Sakr, Ayman Helmy, Eman Khashaba

275-279

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Metabolic derangements in IUGR neonates detected at birth using UPLC-MS

M.A. Abd El-Wahed, O.G. El-Farghali, H.S.A. ElAbd, E.D. El-Desouky, S.M. Hassan

281-287

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PAX5α and PAX5β mRNA expression in breast Cancer: Relation to serum P53 and MMP2

Manal Basyouni Ahmed, Enas Samir Nabih, Muneera Al-Sheeha

289-294

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Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases

Solaf M. Elsayed, Nagia Fahmy, Radwa Gamal, Mohamed Wafik, Dina Zamzam, Mai Fahmy, Mahmoud Suelam

295-298

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Progressive pseudorheumatoid dysplasia in North and West Africa: Clinical description in ten patients with mutations of WISP3

Eliane Chouery, Sandra Corbani, Jaleleddine Dahmen, Leila Zouari, Moez Gribaa, Nadia Leban, Jemni Ben Chibani, Gérard Lefranc, Ali Saad, Amel Haj Khelil, Andoni Urtizberea, André Mégarbané

299-303

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Molecular genetic analysis of Type II diabetes associated m.3243A>G mitochondrial DNA mutation in a Pakistani family

Saidul Abrar, Khushi Muhammad, Hasnain Zaman, Suleman Khan, Faisal Nouroz, Nousheen Bibi

305-308

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 18 No. 3 (2017) / Articles

Articles

Gene frequencies of ABO and Rh blood groups in Nigeria: A review

A prospective longitudinal study to estimate the prevalence of obesity in Egyptian children with nocturnal enuresis and the association between body mass index and response to therapy

CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma

Vitamin D receptor gene variants in Parkinson’s disease patients

Long noncoding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1): A molecular predictor of poor survival in glioblastoma multiforme in Egyptian patients

Association analysis of polymorphisms in EGFR, HER2, ESR1 and THRA genes with coronary artery diseases

Clinical and genetic assessment of pediatric patients with Gaucher’s disease in Upper Egypt

Prevalence of food addiction and its relationship to body mass index

Effect of ABCB1 (3435C>T) and CYP3A5 (6986A>G) genes polymorphism on tacrolimus concentrations and dosage requirements in liver transplant patients

Vitamin D status, receptor gene BsmI (A/G) polymorphism and breast cancer in a group of Egyptian females

Contribution of coagulation factor VII R353Q polymorphism to the risk of thrombotic disorders development (venous and arterial): A case-control study

Metabolic derangements in IUGR neonates detected at birth using UPLC-MS

PAX5α and PAX5β mRNA expression in breast Cancer: Relation to serum P53 and MMP2

Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases

Progressive pseudorheumatoid dysplasia in North and West Africa: Clinical description in ten patients with mutations of WISP3

Molecular genetic analysis of Type II diabetes associated m.3243A>G mitochondrial DNA mutation in a Pakistani family

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