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  • Faith facility improved

    The University of Leicester has refurbished a faith facility for the benefit of its students and other users.

  • Daan van Helden

    Good luck, Victoria! It won’t be the samian without you. Posted by Daan van Helden in The Arch-I-Scan Project on June 5, 2023 please click here to go to the blog post on the Arch-I-Scan news website.

  • Henrik Melin

    Henrik Melin is a post-doc in the Radio and Space Plasma Physics group in the Department of Physics & Astronomy at the University of Leicester.

  • Events

    Find more information on the events hosted by the Centre for New Writing. Events are usually open to the public and free of charge.

  • Solving a century-old problem – Ross Parry explains the importance of Museum Data Service

    Thursday 13 September 2024 marked the launch of a landmark digital service within the UK’s museum sector.

  • Latest insights into Saturn's weird magnetic field only make things weirder

    Leicester space scientists, who have been involved in the Cassini mission for decades, discuss the ‘gold mine’ of information the mission has revealed about the ringed planet and their personal connections to the project

  • Meet our Academic Leads 专业负责人

    Our team of world-leading experts and programme leaders will guide and support students at the Leicester International Institute, Dalian University of Technology across three degree programmes.

  • Assessment and re-assessment (6.22-6.46)

    Read about assessment and re-assessment regulations in Senate Regulation 6.

  • News and publications

    A selection of publications and recent press releases on microbiology or microbiology-related subjects that highlight the impact of the LeMID (Leicester microbial sciences and infectious diseases) Centre, as part of the University of Leicester.

  • Leicester experts contribute to international consortium helping patients with rare disease diagnosis

    Experts from the University of Leicester have co-coordinated a European consortium of 300 researchers to help patients with unsolved rare diseases receive a diagnosis through new genetic reanalysis

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