Search Results - Yitsege, Gelila

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  1. 1
    Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome

    Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome by Karpinski, Beverly A, Maynard, Thomas M, Bryan, Corey A, Yitsege, Gelila, Horvath, Anelia, Lee, Norman H, Moody, Sally A, LaMantia, Anthony-Samuel

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  2. 2
    Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

    Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome by Welby, Lauren, Caudill, Hailey, Yitsege, Gelila, Hamad, Ali, Bunyak, Filiz, Zohn, Irene E, Maynard, Thomas, LaMantia, Anthony-Samuel, Mendelowitz, David, Lever, Teresa E

    Published in Frontiers in neurology
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  3. 3
    Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome

    Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome by Yitsege, Gelila, Stokes, Bethany A., Sabatino, Julia A., Sugrue, Kelsey F., Banyai, Gabor, Paronett, Elizabeth M., Karpinski, Beverly A., Maynard, Thomas M., LaMantia, Anthony‐S., Zohn, Irene E.

    Published in Birth defects research
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