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Genetics and Molecular Research : GMR|August 14, 2014
Bias toward a 1:1 ratio in primer-introduced restriction analysis PCR: mechanism and minimizationS Denden, H Abaidi, M H Hamdaoui, et al.Genetics and Molecular Research : GMR|May 14, 2016
Gender and ethnicity modify the association between the CYP1A2 rs762551 polymorphism and habitual coffee intake: evidence from a meta-analysisS Denden, B Bouden, A Haj Khelil, et al.Annales De Biologie Clinique|August 6, 2009
[Biochemical and molecular diagnosis of alpha 1 antitrypsin deficiency in a Tunisian family]S Denden, W Braham, F Amri, et al.Revue Des Maladies Respiratoires|June 14, 2015
[COPD characteristics in subjects carrying the rare alpha-1 antitrypsin variant PIMMmalton]S Denden, B Bouden, N Boudawara Keskes, et al.Genetics and Molecular Research : GMR|September 9, 2015
Mn-SOD 47 CC genotype in combination with high tea consumption may prevent complications in Tunisian type-2 diabetesH Abaidi, S Denden, A Ghazouani, et al.Genetics and Molecular Research : GMR|May 15, 2010
Relationship between glutathione S-transferase P1 polymorphisms and chronic obstructive pulmonary disease in a Tunisian populationR Lakhdar, S Denden, J Knani, et al.Annales De Biologie Clinique|August 30, 2008
[Alpha 1 antitrypsin polymorphism associated to asthma and emphysema in a central Tunisian population]A Haj-Khelil, S Denden, L Hlioui, et al.Pathologie-Biologie|November 23, 2007
Alpha 1 antitrypsin polymorphism in the Tunisian population with special reference to pulmonary diseaseS Denden, A Haj Khelil, P Perrin, et al.Annales De Biologie Clinique|May 16, 2007
[C3 complement polymorphism in patients suffering from obstructive chronic bronchopneumopathy in Tunisia]N Leban, A Haj Khelil, H Daimi, et al.Annales De Biologie Clinique|August 10, 2000
[Molecular analysis and prenatal diagnosis of beta-thalassemia: about our experience in central Tunisia]S Laradi, A Haj Khelil, H Omri, et al.Pageof 2