Résultats de la recherche

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Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome
Missense mutation in the second RNA binding domain reveals a role for Prkra (PACT/RAX) during skull development
Deletion of the App-Runx1 region in mice models human partial monosomy 21
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics