Lack of association between genetic variants in the 19q13.32 region and CHD risk in the Algerian population: a population-based nested case-control study

por Boulenouar, Houssam, Hetraf, Sarah Aicha Lardjam, Djellouli, Hadjira Ouhaibi, Meroufel, Djabaria Naima, Fodil, Faouzia Zemani, Hammani-Medjaoui, Imane, Mehtar, Nadhira Saidi, Houti, Leila, Benchekor, Sounnia Mediene
Publicado 2020

Association of IL4 rs2070874, FoxP3 rs3761548 Polymorphisms with Keratoconus in Algeria

por Meteoukki, Wafaa, Fodil, Mostefa, Negaz, Nawel Adda, Rahmoun, Nesrine, Hetraf, Sarah Lardjam, Djellouli, Hadjira Ouhaibi, Messal, Ahlem Djelti, Abdi, Meriem, Aberkane, Meriem Samia, Chiali, Abdelillah, Derdour, Amine, Idder, Aicha, -Fodil, Faouzia Zemani
Publicado 2021