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Issue Title
Vol 10, No 2 (2009) The frequency of consanguineous marriages and their effects on offsprings in Tabriz city Abstract   PDF
F Aboualsoltani, SA Rahmani, M Pourbarghi, H Dolatkhah, AM Aghazadeh
Vol 9, No 1 (2008) The Impact of Prenatal Diagnosis in Egyptian Families with Duchenne Muscular Dystrophy Abstract   PDF
LK Effat, KS Amr, AA El-Harouni, KR Gaber
Vol 18, No 1 (2017) The β fibrinogen gene G-455A polymorphism in Asian subjects with coronary heart disease: A meta analysis Abstract   PDF
Jonny Karunia Fajar
Vol 13, No 3 (2012) The methylenetetrahydrofolate reductase gene variant (C677T) in risk mothers with Down syndrome among Saudi population Abstract   PDF
MT Tayeb
Vol 16, No 2 (2015) The population structure of Ukraine in relation to the phenylthiocarbamide sensitivity Abstract   PDF
OV Filiptsova, IA Timoshyna, YN Kobets, MN Kobets, IS Burlaka, IA Hurko
Vol 15, No 2 (2014) The promoter region (G-800A and C-509T) polymorphisms of transforming growth factor-β1 gene among young women with recurrent urinary tract infection Abstract   PDF
M Syukri, M Sja’bani, MHNE Soesatyo, I Astuti, I Imran, H Harapan
Vol 16, No 4 (2015) The relation between antihistamine medication during early pregnancy & birth defects Abstract   PDF
Rabah M Shawky, Neveen S Seifeldin
Vol 19, No 1 (2018) The relation of thrombomodulin G33A and C1418T gene polymorphisms to the risk of acute myocardial infarction in Egyptians Abstract   PDF
Wael Alkhiary, Mohamed Abdalaal, Amr Mohamed El-Saddik
Vol 15, No 2 (2014) The response of skin hardness and pain sensation to ultrasonic treatment in lipodermatosclerosis patients Abstract   PDF
SA Hamid, ZM Ibrahim Ali, HM Mohamady
Vol 16, No 4 (2015) The role of microRNAs on angiogenesis and vascular pressure in preeclampsia: The evidence from systematic review Abstract   PDF
Harapan Harapan, Cut M Yeni
Vol 19, No 2 (2018) The V279F polymorphism might change protein character and immunogenicity in Lp-PLA2 protein Abstract   PDF
Widodo Widodo, Anggia Noor Ramadhani, Anissa Nofitasari, Sapti Puspitarini, Didik Priyandoko, Mohammad Saifur Rohman, Mifetika Lukitasari
Vol 10, No 2 (2009) Therapeutic approaches to genetic disorders Abstract   PDF
MS Zaghloul, SM Elsayed, HAA Hosseny
Vol 12, No 2 (2011) Thiopurine S-methyltransferase genetic polymorphism in the Tunisian population Abstract   PDF
LB Salah, CB Salem, F B’Chir, K Bouraoui, F Broly, S Saguem
Vol 17, No 3 (2016) Treatment options for patients with Gaucher disease Abstract   PDF
Rabah M Shawky, Solaf M Elsayed
Vol 10, No 1 (2009) Triple A syndrome presenting with myopathy: An Egyptian patient Abstract   PDF
RM Shawky, SM Elsayed, HH Elsedfy
Vol 10, No 2 (2009) Trisomy 9 syndrome in a neonate with unusual features Abstract   PDF
MMA Henedi, FM Mohammed, HA Masoud, SJ Abualhasan, SA Al Awadi
Vol 18, No 2 (2017) Two Libyan siblings with beta-ketothiolase deficiency: A case report and review of literature Abstract   PDF
Elsayed Abdelkreem, Hanna Alobaidy, Yuka Aoyama, Shaimaa Mahmoud, Mohamed Abd El Aal, Toshiyuki Fukao
Vol 15, No 3 (2014) Unilateral proximal focal femoral deficiency, fibular aplasia, tibial campomelia and oligosyndactyly in an Egyptian child – Probable FFU syndrome Abstract   PDF
R M Shawky, H S Abd Elkhalek, S Gad, S A Mohammad
Vol 13, No 3 (2012) Use of denaturing gradient gel electrophoresis in screening unknown β-thalassemia mutations in Egyptian patients Abstract   PDF
G Christopoulos, GM Ezzat, M Kleanthous
Vol 13, No 3 (2012) Virologic response at week 8 of combined treatment as a predictor of sustained virologic response in non rapid virologic response, chronic HCV genotype 4 infected patients Abstract   PDF
A Monis, AA Monis, R Al Swaff
Vol 18, No 3 (2017) Vitamin D receptor gene variants in Parkinson’s disease patients Abstract   PDF
Rokhsareh Meamar, Seyed Morteza Javadirad, Niloofar Chitsaz, Mojgan Asadian Ghahfarokhi, Mehdi Kazemi, Maryam Ostadsharif
Vol 18, No 3 (2017) Vitamin D status, receptor gene BsmI (A/G) polymorphism and breast cancer in a group of Egyptian females Abstract   PDF
Rasha Rizk Elzehery, Azza A. Baiomy, Mohamed AbdEl-Fattah Hegazy, Rami Fares, Abdel-Hady El-Gilany, Refaat Hegazi
Vol 17, No 3 (2016) Wolman disease in patients with familial hemophagocytic lymphohistiocytosis (FHL) negative mutations Abstract   PDF
Solaf Elsayed, Ezzat Elsobky, Azza Tantawy, Eman Ragab, Marine Gil, Nathalie Lambert, Geneviéve de Saint Basile
Vol 16, No 2 (2015) XmnI polymorphism: Relation to β-thalassemia phenotype and genotype in Egyptian Children Abstract   PDF
F Said, A Abdel-Salam
Vol 19, No 2 (2018) XRCC1 Arg194Trp polymorphism is no risk factor for skin cancer development in Kashmiri population Abstract   PDF
Rouf Maqbool, Shajrul Amin, Sabhiya Majeed, Aaliya Bhat, Shayaq ul Abeer Rasool, Mudasar Nabi
Vol 19, No 3 (2018) Yield of karyotyping in children with developmental delay and/or dysmorphic features in Sohag University Hospital, Upper Egypt Abstract   PDF
Abdelrahim A. Sadek, Mostafa Ashry Mohamed
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ISSN: 1110-8630
AJOL African Journals Online