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Xizmatlar

Corinne Cruaud

3 ta ish

French National Sequencing Center

AkademScholarda batafsil koʻrsatkichlar

  1. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

    Marianne Abifadel, Mathilde Varret, Jean‐Pierre Rabès +23

    Maqola20033 iqtibos
    ABI

  2. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

    Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont +27

    Maqola20032 iqtibos
    ABI

  3. Positive selection of protective variants for type 2 diabetes from the Neolithic onward: a case study in Central Asia

    Laure Ségurel, Frédéric Austerlitz, Bruno Toupance +12

    MaqolaOchiq kirishGenetic Associations and EpidemiologyEuropean Journal of Human Genetics20131 iqtibos
    ABI