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Dive into the research topics of 'Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-γ receptor 1 deficiency'. Together they form a unique fingerprint.- Sort by
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Carolina Prando, Stéphanie Boisson-Dupuis, Audrey V. Grant, Xiao Fei Kong, Jacinta Bustamante, Jacqueline Feinberg, Ariane Chapgier, Yoann Rose, Lucile Jannière, Elena Rizzardi, Qiuping Zhang, Catherine M. Shanahan, Louis Viollet, Stanislas Lyonnet, Laurent Abel, Ezia Maria Ruga, Jean Laurent Casanova
Research output: Contribution to journal › Article › peer-review