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Human Molecular Genetics|April 25, 2015
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the ciliumJosé A Caparrós-Martín, Alessandro De Luca, François Cartault, et al.
La Tunisie Medicale|June 1, 2026
Percutaneous coronary intervention of chronic total occlusion: A 5-year monocentric experience [cite: 62]Selim Boudiche, Mouna Bader, Manel Abbassi, et al.
Clinical Dysmorphology|August 28, 2025
Monoallelic variants in ACVR1 in a cohort of Egyptian individuals with fibrodysplasia ossificans progressivaRasha M Elhossini, Hala T El-Bassyouni, Engy A Ashaat, et al.
Emerging Infectious Diseases|June 8, 2007
Genome analysis linking recent European and African influenza (H5N1) virusesSteven L Salzberg, Carl Kingsford, Giovanni Cattoli, et al.
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association|January 27, 2022
The egyptian clinical practice guidelines for the diagnosis and management of metabolic associated fatty liver diseaseYasser Fouad, Gamal Esmat, Reda Elwakil, et al.
American Journal of Human Genetics|October 15, 2020
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation SyndromeAdrian Palencia-Campos, Phillip C Aoto, Erik M F Machal, et al.
Anaesthesia, Critical Care & Pain Medicine|May 23, 2025
Pain intensity after robotic-assisted urological surgery: the PAIROU study an international prospective cohort studyPauline Rouxel, Emilien Rayon, Anne-Sophie Bellocq, et al.
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